Basb027 proteins and genes from moraxella catarrhalis, antigens, antibodies, and uses

ABSTRACT

The invention provides BASB027 polypeptides and polynucleotides encoding BASB027 polypeptides and methods for producing such polypeptides by recombinant techniques. Also provided are diagnostic, prophylactic and therapeutic uses.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional application of U.S. patent applicationSer. No. 10/896,725, filed Jul. 22, 2004, now allowed, which applicationis a divisional of U.S. patent application Ser. No. 09/701,711 filedJul. 27, 2001, now issued as U.S. Pat. No. 6,803,043 on Oct. 12, 2004,which is a national stage application filed under 35 U.S.C.§371 ofInternational Application No. PCT/EP99/03822, accorded an internationalfiling date of May 31, 1999, which claims the benefit of Great BritainPatent Application Nos. 9811945.6, filed Jun. 3, 1998 and 9905304.3,filed Mar. 8, 1999. All the aforementioned applications are hereinincorporated by reference in their entirety.

STATEMENT REGARDING SEQUENCE LISTING

The Sequence Listing associated with this application is provided intext format in lieu of a paper copy, and is hereby incorporated byreference into the specification. The name of the text file containingthe Sequence Listing is 400077_(—)404D2_SEQUENCE_LISTING.txt. The textfile is 22 KB, was created on Nov. 18, 2009 and is being submittedelectronically via EFS-Web.

FIELD OF THE INVENTION

This invention relates to polynucleotides, (herein referred to as“BASB027 polynucleotide(s)”), polypeptides encoded by them (referred toherein as “BASB027” or “BASB027 polypeptide(s)”), recombinant materialsand methods for their production. In another aspect, the inventionrelates to methods for using such polypeptides and polynucleotides,including vaccines against bacterial infections. In a further aspect,the invention relates to diagnostic assays for detecting infection ofcertain pathogens.

BACKGROUND OF THE INVENTION

Moraxella catarrhalis (also named Branhamella catarrhalis) is a Gramnegative bacteria frequently isolated from the human upper respiratorytract. It is responsible for several pathologies the main ones beingotitis media in infants and children, and pneumonia in elderlies. It isalso responsible of sinusitis, nosocomial infections and less frequentlyof invasive diseases.

Otitis media is an important childhood disease both by the number ofcases and its potential sequelae. More than 3.5 millions cases arerecorded every year in the United States, and it is estimated that 80%of the children have experienced at least one episode of otitis beforereaching the age of 3 (Klein, J O (1994) Clin. Inf. Dis. 19:823). Leftuntreated, or becoming chronic, this disease may lead to hearing lossesthat could be temporary (in the case of fluid accumulation in the middleear) or permanent (if the auditive nerve is damaged). In infants, suchhearing losses may be responsible for a delayed speech learning.

Three bacterial species are primarily isolated from the middle ear ofchildren with otitis media: Streptococcus pneumoniae, non typeableHaemophilus influenza (NTHi) and M. catarrhalis. They are present in 60to 90% of the cases. A review of recent studies shows that S. pneumoniaeand NTHi represent both about 30%, and M. catarrhalis about 15% of theotitis media cases (Murphy, T F (1996) Microbiol. Rev. 60:267). Otherbacteria could be isolated from the middle ear (H. influenza type B, S.pyogenes etc) but at a much lower frequency (2% of the cases or less).

Epidemiological data indicate that, for the pathogens found in themiddle ear, the colonization of the upper respiratory tract is anabsolute prerequisite for the development of an otitis; other arehowever also required to lead to the disease (Dickinson, D P et al.(1988) J. Infect. Dis. 158:205, Faden, H L et al. (1991) Ann. Otorhinol.Laryngol. 100:612). These are important to trigger the migration of thebacteria into the middle ear via the Eustachian tubes, followed by theinitiation of an inflammatory process. These factors are unknown todate. It has been postulated that a transient anomaly of the immunesystem following a viral infection, for example, could cause aninability to control the colonization of the respiratory tract (Faden, HL et al (1994) J. Infect. Dis. 169:1312). An alternative explanation isthat the exposure to environmental factors allow a more importantcolonization of some children, who subsequently become susceptible tothe development of otitis media because of the sustained presence ofmiddle ear pathogens (Murphy, T F (1996) Microbiol. Rev. 60:267).

The immune response to M. catarrhalis is poorly characterized. Theanalysis of strains isolated sequentially from the nasopharynx of babiesfollowed from 0 to 2 years of age, indicates that they get and eliminatefrequently new strains. This indicates that an efficacious immuneresponse against this bacteria is mounted by the colonized children(Faden, H L et al (1994) J. Infect. Dis. 169:1312).

In most adults tested, bactericidal antibodies have been identified(Chapman, A J et al. (1985) J. Infect. Dis. 151:878). Strains of M.catarrhalis present variations in their capacity to resist serumbactericidal activity: in general, isolates from diseased individualsare more resistant than those who are simply colonized (Hol, C et al.(1993) Lancet 341:1281, Jordan, K L et al. (1990) Am. J. Med. 88 (suppl.5A):28S). Serum resistance could therefore be considered as a virulencefactor of the bacteria. An opsonizing activity has been observed in thesera of children recovering from otitis media.

The antigens targetted by these different immune responses in humanshave not been identified, with the exception of OMP B1, a 84 kDa proteinwhich expression is regulated by iron, and that is recognized by thesera of patients with pneumonia (Sethi, S, et al. (1995) Infect. Immun.63:1516), and of UspA1 and UspA2 (Chen D. et al. (1999), Infect. Immun.67:1310).

A few other membrane proteins present on the surface of M. catarrhalishave been characterized using biochemical method, or for their potentialimplication in the induction of a protective immunity (for review, seeMurphy, T F (1996) Microbiol. Rev. 60:267). In a mouse pneumonia model,the presence of antibodies raised against some of them (UspA, CopB)favors a faster clearance of the pulmonary infection. Anotherpolypeptide (OMP CD) is highly conserved among M. catarrhalis strains,and presents homologies with a porin of Pseudomonas aeruginosa, whichhas been demonstrated efficacious against this bacterium in animalmodels.

The frequency of Moraxella catarrhalis infections has risen dramaticallyin the past few decades. This has been attributed to the emergence ofmultiply antibiotic resistant strains and an increasing population ofpeople with weakened immune systems. It is no longer uncommon to isolateMoraxella catarrhalis strains that are resistant to some or all of thestandard antibiotics. This phenomenon has created an unmet medical needand demand for new anti-microbial agents, vaccines, drug screeningmethods, and diagnostic tests for this organism.

SUMMARY OF THE INVENTION

The present invention relates to BASB027, in particular BASB027polypeptides and BASB027 polynucleotides, recombinant materials andmethods for their production. In another aspect, the invention relatesto methods for using such polypeptides and polynucleotides, includingprevention and treatment of microbial diseases, amongst others. In afurther aspect, the invention relates to diagnostic assays for detectingdiseases associated with microbial infections and conditions associatedwith such infections, such as assays for detecting expression oractivity of BASB027 polynucleotides or polypeptides.

Various changes and modifications within the spirit and scope of thedisclosed invention will become readily apparent to those skilled in theart from reading the following descriptions and from reading the otherparts of the present disclosure.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A-1L show photographs of electrophoresis gels obtained in theRFLP analysis of BASB027.

FIGS. 2A-2G show consecutive, aligned sequences for two BASB027polynucleotides.

FIGS. 3A-3C show consecutive, aligned sequences for two BASB027polypeptides.

FIG. 4 shows a Coomassie stained SDS-polyacrylamide gel of purifiedBASB027 protein.

FIG. 5 shows a Western blot of purified BASB027 probed with anti-Hisantibody.

FIG. 6 shows a Western blot of purified BASB027 protein probed with thecorresponding anti-recombinant sera. Panel A: pre-immune serum. Panel B:immune serum.

FIGS. 7A and 7B show Western blots of whole cell lysates of 16 strainsof M. catarrhalis using pooled sera against the BASB027 protein (serawas diluted at 1:2000).

FIG. 8 shows a Western blot of purified, recombinant BASB027 withcorresponding anti-peptide sera. Lanes 2 and 3 non immune sera. Lanes 1and 4 immune sera.

DESCRIPTION OF THE INVENTION

The invention relates to BASB027 polypeptides and polynucleotides asdescribed in greater detail below. In particular, the invention relatesto polypeptides and polynucleotides of BASB027 of Moraxella catarrhalis,which is related by amino acid sequence homology to Neisseriameningitidis OMP85 outer membrane protein. The invention relatesespecially to BASB027 having the nucleotide and amino acid sequences setout in SEQ ID NO:1 or 3 and SEQ ID NO:2 or 4 respectively. It isunderstood that sequences recited in the Sequence Listing below as “DNA”represent an exemplification of one embodiment of the invention, sincethose of ordinary skill will recognize that such sequences can beusefully employed in polynucleotides in general, includingribopolynucleotides.

Polypeptides

In one aspect of the invention there are provided polypeptides ofMoraxella catarrhalis referred to herein as “BASB027” and “BASB027polypeptides” as well as biologically, diagnostically, prophylactically,clinically or therapeutically useful variants thereof, and compositionscomprising the same.

The present invention further provides for:

(a) an isolated polypeptide which comprises an amino acid sequence whichhas at least 85% identity, preferably at least 90% identity, morepreferably at least 95% identity, most preferably at least 97-99% orexact identity, to that of SEQ ID NO:2 or 4;

(b) a polypeptide encoded by an isolated polynucleotide comprising apolynucleotide sequence which has at least 85% identity, preferably atleast 90% identity, more preferably at least 95% identity, even morepreferably at least 97-99% or exact identity to SEQ ID NO:1 or 3 overthe entire length of SEQ ID NO:1 or 3 respectively; or

(c) a polypeptide encoded by an isolated polynucleotide comprising apolynucleotide sequence encoding a polypeptide which has at least 85%identity, preferably at least 90% identity, more preferably at least 95%identity, even more preferably at least 97-99% or exact identity, to theamino acid sequence of SEQ ID NO:2 or 4.

The BASB027 polypeptides provided in SEQ ID NO:2 or 4 are the BASB027polypeptides from Moraxella catarrhalis strain Mc2931 (ATCC 43617).

The invention also provides an immunogenic fragment of a BASB027polypeptide, that is, a contiguous portion of the BASB027 polypeptidewhich has the same or substantially the same immunogenic activity as thepolypeptide comprising the amino acid sequence of SEQ ID NO:2 or 4. Thatis to say, the fragment (if necessary when coupled to a carrier) iscapable of raising an immune response which recognises the BASB027polypeptide. Such an immunogenic fragment may include, for example, theBASB027 polypeptide lacking an N-terminal leader sequence, and/or atransmembrane domain and/or a C-terminal anchor domain. In a preferredaspect the immunogenic fragment of BASB027 according to the inventioncomprises substantially all of the extracellular domain of a polypeptidewhich has at least 85% identity, preferably at least 90% identity, morepreferably at least 95% identity, most preferably at least 97-99%identity, to that of SEQ ID NO:2 or 4 over the entire length of SEQ IDNO:2.

A fragment is a polypeptide having an amino acid sequence that isentirely the same as part but not all of any amino acid sequence of anypolypeptide of the invention. As with BASB027 polypeptides, fragmentsmay be “free-standing,” or comprised within a larger polypeptide ofwhich they form a part or region, most preferably as a single continuousregion in a single larger polypeptide.

Preferred fragments include, for example, truncation polypeptides havinga portion of an amino acid sequence of SEQ ID NO:2 or 4 or of variantsthereof, such as a continuous series of residues that includes an amino-and/or carboxyl-terminal amino acid sequence. Degradation forms of thepolypeptides of the invention produced by or in a host cell, are alsopreferred. Further preferred are fragments characterized by structuralor functional attributes such as fragments that comprise alpha-helix andalpha-helix forming regions, beta-sheet and beta-sheet-forming regions,turn and turn-forming regions, coil and coil-forming regions,hydrophilic regions, hydrophobic regions, alpha amphipathic regions,beta amphipathic regions, flexible regions, surface-forming regions,substrate binding region, and high antigenic index regions.

Further preferred fragments include an isolated polypeptide comprisingan amino acid sequence having at least 15, 20, 30, 40, 50 or 100contiguous amino acids from the amino acid sequence of SEQ ID NO:2 or 4,or an isolated polypeptide comprising an amino acid sequence having atleast 15, 20, 30, 40, 50 or 100 contiguous amino acids truncated ordeleted from the amino acid sequence of SEQ ID NO:2 or 4.

Fragments of the polypeptides of the invention may be employed forproducing the corresponding full-length polypeptide by peptidesynthesis; therefore, these fragments may be employed as intermediatesfor producing the full-length polypeptides of the invention.

Particularly preferred are variants in which several, 5-10, 1-5, 1-3,1-2 or 1 amino acids are substituted, deleted, or added in anycombination.

The polypeptides, or immunogenic fragments, of the invention may be inthe form of the “mature” protein or may be a part of a larger proteinsuch as a precursor or a fusion protein. It is often advantageous toinclude an additional amino acid sequence which contains secretory orleader sequences, pro-sequences, sequences which aid in purificationsuch as multiple histidine residues, or an additional sequence forstability during recombinant production. Furthermore, addition ofexogenous polypeptide or lipid tail or polynucleotide sequences toincrease the immunogenic potential of the final molecule is alsoconsidered.

In one aspect, the invention relates to genetically engineered solublefusion proteins comprising a polypeptide of the present invention, or afragment thereof, and various portions of the constant regions of heavyor light chains of immunoglobulins of various subclasses (IgG, IgM, IgA,IgE). Preferred as an immunoglobulin is the constant part of the heavychain of human IgG, particularly IgG1, where fusion takes place at thehinge region. In a particular embodiment, the Fc part can be removedsimply by incorporation of a cleavage sequence which can be cleaved withblood clotting factor Xa.

Furthermore, this invention relates to processes for the preparation ofthese fusion proteins by genetic engineering, and to the use thereof fordrug screening, diagnosis and therapy. A further aspect of the inventionalso relates to polynucleotides encoding such fusion proteins. Examplesof fusion protein technology can be found in International PatentApplication Nos. WO94/29458 and WO94/22914.

The proteins may be chemically conjugated, or expressed as recombinantfusion proteins allowing increased levels to be produced in anexpression system as compared to non-fused protein. The fusion partnermay assist in providing T helper epitopes (immunological fusionpartner), preferably T helper epitopes recognised by humans, or assistin expressing the protein (expression enhancer) at higher yields thanthe native recombinant protein. Preferably the fusion partner will beboth an immunological fusion partner and expression enhancing partner.

Fusion partners include protein D from Haemophilus influenzae and thenon-structural protein from influenzae virus, NS1 (hemagglutinin).Another fusion partner is the protein known as LytA. Preferably the Cterminal portion of the molecule is used. Lyta is derived fromStreptococcus pneumoniae which synthesize an N-acetyl-L-alanine amidase,amidase LytA, (coded by the lytA gene {Gene, 43 (1986) page 265-272}) anautolysin that specifically degrades certain bonds in the peptidoglycanbackbone. The C-terminal domain of the LytA protein is responsible forthe affinity to the choline or to some choline analogues such as DEAE.This property has been exploited for the development of E. coli C-LytAexpressing plasmids useful for expression of fusion proteins.Purification of hybrid proteins containing the C-LytA fragment at itsamino terminus has been described {Biotechnology: 10, (1992) page795-798}. It is possible to use the repeat portion of the LytA moleculefound in the C terminal end starting at residue 178, for exampleresidues 188-305.

The present invention also includes variants of the aforementionedpolypeptides, that is polypeptides that vary from the referents byconservative amino acid substitutions, whereby a residue is substitutedby another with like characteristics. Typical such substitutions areamong Ala, Val, Leu and Ile; among Ser and Thr; among the acidicresidues Asp and Glu; among Asn and Gln; and among the basic residuesLys and Arg; or aromatic residues Phe and Tyr.

Polypeptides of the present invention can be prepared in any suitablemanner. Such polypeptides include isolated naturally occurringpolypeptides, recombinantly produced polypeptides, syntheticallyproduced polypeptides, or polypeptides produced by a combination ofthese methods. Means for preparing such polypeptides are well understoodin the art.

It is most preferred that a polypeptide of the invention is derived fromMoraxella catarrhalis, however, it may preferably be obtained from otherorganisms of the same taxonomic genus. A polypeptide of the inventionmay also be obtained, for example, from organisms of the same taxonomicfamily or order.

Polynucleotides

It is an object of the invention to provide polynucleotides that encodeBASB027 polypeptides, particularly polynucleotides that encode thepolypeptide herein designated BASB027.

In a particularly preferred embodiment of the invention thepolynucleotide comprises a region encoding BASB027 polypeptidescomprising a sequence set out in SEQ ID NO:1 or 3 which includes a fulllength gene, or a variant thereof.

The BASB027 polynucleotides provided in SEQ ID NO:1 or 3 are the BASB027polynucleotides from Moraxella catarrhalis strain Mc2931 (ATCC 43617).

As a further aspect of the invention there are provided isolated nucleicacid molecules encoding and/or expressing BASB027 polypeptides andpolynucleotides, particularly Moraxella catarrhalis BASB027 polypeptidesand polynucleotides, including, for example, unprocessed RNAs, ribozymeRNAs, mRNAs, cDNAs, genomic DNAs, B- and Z-DNAs. Further embodiments ofthe invention include biologically, diagnostically, prophylactically,clinically or therapeutically useful polynucleotides and polypeptides,and variants thereof, and compositions comprising the same.

Another aspect of the invention relates to isolated polynucleotides,including at least one full length gene, that encodes a BASB027polypeptide having a deduced amino acid sequence of SEQ ID NO:2 or 4 andpolynucleotides closely related thereto and variants thereof.

In another particularly preferred embodiment of the invention there is aBASB027 polypeptide from Moraxella catarrhalis comprising or consistingof an amino acid sequence of SEQ ID NO:2 or 4 or a variant thereof.

Using the information provided herein, such as a polynucleotide sequenceset out in SEQ ID NO:1 or 3, a polynucleotide of the invention encodingBASB027 polypeptide may be obtained using standard cloning and screeningmethods, such as those for cloning and sequencing chromosomal DNAfragments from bacteria using Moraxella catarrhalis Catlin cells asstarting material, followed by obtaining a full length clone. Forexample, to obtain a polynucleotide sequence of the invention, such as apolynucleotide sequence given in SEQ ID NO:1 or 3, typically a libraryof clones of chromosomal DNA of Moraxella catarrhalis Catlin in E. colior some other suitable host is probed with a radiolabeledoligonucleotide, preferably a 17-mer or longer, derived from a partialsequence. Clones carrying DNA identical to that of the probe can then bedistinguished using stringent hybridization conditions. By sequencingthe individual clones thus identified by hybridization with sequencingprimers designed from the original polypeptide or polynucleotidesequence it is then possible to extend the polynucleotide sequence inboth directions to determine a full length gene sequence. Conveniently,such sequencing is performed, for example, using denatured doublestranded DNA prepared from a plasmid clone. Suitable techniques aredescribed by Maniatis, T., Fritsch, E. F. and Sambrook et al., MOLECULARCLONING, A LABORATORY MANUAL, 2nd Ed.; Cold Spring Harbor LaboratoryPress, Cold Spring Harbor, N.Y. (1989). (see in particular Screening ByHybridization 1.90 and Sequencing Denatured Double-Stranded DNATemplates 13.70). Direct genomic DNA sequencing may also be performed toobtain a full length gene sequence. Illustrative of the invention, eachpolynucleotide set out in SEQ ID NO:1 or 3 was discovered in a DNAlibrary derived from Moraxella catarrhalis.

Moreover, each DNA sequence set out in SEQ ID NO:1 or 3 contains an openreading frame encoding a protein having about the number of amino acidresidues set forth in SEQ ID NO:2 or 4 with a deduced molecular weightthat can be calculated using amino acid residue molecular weight valueswell known to those skilled in the art.

The polynucleotide of SEQ ID NO:1, between the start codon at nucleotidenumber 1 and the stop codon which begins at nucleotide number 2440 ofSEQ ID NO:1, encodes the polypeptide of SEQ ID NO:2.

The polynucleotide of SEQ ID NO:3, between the start codon at nucleotidenumber 1 and the stop codon which begins at nucleotide number 2440 ofSEQ ID NO:3, encodes the polypeptide of SEQ ID NO:4.

In a further aspect, the present invention provides for an isolatedpolynucleotide comprising or consisting of:

(a) a polynucleotide sequence which has at least 85% identity,preferably at least 90% identity, more preferably at least 95% identity,even more preferably at least 97-99% or exact identity to SEQ ID NO:1 or3 over the entire length of SEQ ID NO:1 or 3 respectively; or

(b) a polynucleotide sequence encoding a polypeptide which has at least85% identity, preferably at least 90% identity, more preferably at least95% identity, even more preferably at least 97-99% or 100% exact, to theamino acid sequence of SEQ ID NO:2 or 4, over the entire length of SEQID NO:2 or 4 respectively.

A polynucleotide encoding a polypeptide of the present invention,including homologs and orthologs from species other than Moraxellacatarrhalis, may be obtained by a process which comprises the steps ofscreening an appropriate library under stringent hybridizationconditions (for example, using a temperature in the range of 45-65° C.and an SDS concentration from 0.1-1%) with a labeled or detectable probeconsisting of or comprising the sequence of SEQ ID NO:1 or 3 or afragment thereof; and isolating a full-length gene and/or genomic clonescontaining said polynucleotide sequence.

The invention provides a polynucleotide sequence identical over itsentire length to a coding sequence (open reading frame) in SEQ ID NO:1or 3. Also provided by the invention is a coding sequence for a maturepolypeptide or a fragment thereof, by itself as well as a codingsequence for a mature polypeptide or a fragment in reading frame withanother coding sequence, such as a sequence encoding a leader orsecretory sequence, a pre-, or pro- or prepro-protein sequence. Thepolynucleotide of the invention may also contain at least one non-codingsequence, including for example, but not limited to at least onenon-coding 5′ and 3′ sequence, such as the transcribed butnon-translated sequences, termination signals (such as rho-dependent andrho-independent termination signals), ribosome binding sites, Kozaksequences, sequences that stabilize mRNA, introns, and polyadenylationsignals. The polynucleotide sequence may also comprise additional codingsequence encoding additional amino acids. For example, a marker sequencethat facilitates purification of the fused polypeptide can be encoded.In certain embodiments of the invention, the marker sequence is ahexa-histidine peptide, as provided in the pQE vector (QIAGEN, Inc.) anddescribed in Gentz et al., Proc. Natl. Acad. Sci., USA 86: 821-824(1989), or an HA peptide tag (Wilson et al., Cell 37: 767 (1984), bothof which may be useful in purifying polypeptide sequence fused to them.Polynucleotides of the invention also include, but are not limited to,polynucleotides comprising a structural gene and its naturallyassociated sequences that control gene expression.

The nucleotide sequence encoding BASB027 polypeptide of SEQ ID NO:2 or 4may be identical to the polypeptide encoding sequence contained innucleotides 1 to 2439 of SEQ ID NO:1 or 3 respectively. Alternatively itmay be a sequence, which as a result of the redundancy (degeneracy) ofthe genetic code, also encodes the polypeptide of SEQ ID NO:2 or 4.

The term “polynucleotide encoding a polypeptide” as used hereinencompasses polynucleotides that include a sequence encoding apolypeptide of the invention, particularly a bacterial polypeptide andmore particularly a polypeptide of the Moraxella catarrhalis BASB027having an amino acid sequence set out in SEQ ID NO:2 or 4. The term alsoencompasses polynucleotides that include a single continuous region ordiscontinuous regions encoding the polypeptide (for example,polynucleotides interrupted by integrated phage, an integrated insertionsequence, an integrated vector sequence, an integrated transposonsequence, or due to RNA editing or genomic DNA reorganization) togetherwith additional regions, that also may contain coding and/or non-codingsequences.

The invention further relates to variants of the polynucleotidesdescribed herein that encode variants of a polypeptide having a deducedamino acid sequence of SEQ ID NO:2 or 4. Fragments of polynucleotides ofthe invention may be used, for example, to synthesize full-lengthpolynucleotides of the invention.

Further particularly preferred embodiments are polynucleotides encodingBASB027 variants, that have the amino acid sequence of BASB027polypeptide of SEQ ID NO:2 or 4 in which several, a few, 5 to 10, 1 to5, 1 to 3, 2, 1 or no amino acid residues are substituted, modified,deleted and/or added, in any combination. Especially preferred amongthese are silent substitutions, additions and deletions, that do notalter the properties and activities of BASB027 polypeptide.

Further preferred embodiments of the invention are polynucleotides thatare at least 85% identical over their entire length to a polynucleotideencoding BASB027 polypeptide having an amino acid sequence set out inSEQ ID NO:2 or 4, and polynucleotides that are complementary to suchpolynucleotides. Alternatively, most highly preferred arepolynucleotides that comprise a region that is at least 90% identicalover its entire length to a polynucleotide encoding BASB027 polypeptideand polynucleotides complementary thereto. In this regard,polynucleotides at least 95% identical over their entire length to thesame are particularly preferred. Furthermore, those with at least 97%are highly preferred among those with at least 95%, and among thesethose with at least 98% and at least 99% are particularly highlypreferred, with at least 99% being the more preferred.

Preferred embodiments are polynucleotides encoding polypeptides thatretain substantially the same biological function or activity as themature polypeptide encoded by a DNA of SEQ ID NO:1 or 3.

In accordance with certain preferred embodiments of this invention thereare provided polynucleotides that hybridize, particularly understringent conditions, to BASB027 polynucleotide sequences, such as thosepolynucleotides in SEQ ID NO:1 or 3.

The invention further relates to polynucleotides that hybridize to thepolynucleotide sequences provided herein. In this regard, the inventionespecially relates to polynucleotides that hybridize under stringentconditions to the polynucleotides described herein. As herein used, theterms “stringent conditions” and “stringent hybridization conditions”mean hybridization occurring only if there is at least 95% andpreferably at least 97% identity between the sequences. A specificexample of stringent hybridization conditions is overnight incubation at42° C. in a solution comprising: 50% formamide, 5×SSC (150 mM NaCl, 15mM trisodium citrate), 50 mM sodium phosphate (pH7.6), 5×Denhardt'ssolution, 10% dextran sulfate, and 20 micrograms/ml of denatured,sheared salmon sperm DNA, followed by washing the hybridization supportin 0.1×SSC at about 65° C. Hybridization and wash conditions are wellknown and exemplified in Sambrook, et al., Molecular Cloning: ALaboratory Manual, Second Edition, Cold Spring Harbor, N.Y., (1989),particularly Chapter 11 therein. Solution hybridization may also be usedwith the polynucleotide sequences provided by the invention.

The invention also provides a polynucleotide consisting of or comprisinga polynucleotide sequence obtained by screening an appropriate librarycontaining the complete gene for a polynucleotide sequence set forth inSEQ ID NO:1 or 3 under stringent hybridization conditions with a probehaving the sequence of said polynucleotide sequence set forth in SEQ IDNO:1 or 3 or a fragment thereof; and isolating said polynucleotidesequence. Fragments useful for obtaining such a polynucleotide include,for example, probes and primers fully described elsewhere herein.

As discussed elsewhere herein regarding polynucleotide assays of theinvention, for instance, the polynucleotides of the invention, may beused as a hybridization probe for RNA, cDNA and genomic DNA to isolatefull-length cDNAs and genomic clones encoding BASB027 and to isolatecDNA and genomic clones of other genes that have a high identity,particularly high sequence identity, to the BASB027 gene. Such probesgenerally will comprise at least 15 nucleotide residues or base pairs.Preferably, such probes will have at least 30 nucleotide residues orbase pairs and may have at least 50 nucleotide residues or base pairs.Particularly preferred probes will have at least 20 nucleotide residuesor base pairs and will have less than 30 nucleotide residues or basepairs.

A coding region of a BASB027 gene may be isolated by screening using aDNA sequence provided in SEQ ID NO:1 or 3 to synthesize anoligonucleotide probe. A labeled oligonucleotide having a sequencecomplementary to that of a gene of the invention is then used to screena library of cDNA, genomic DNA or mRNA to determine which members of thelibrary the probe hybridizes to.

There are several methods available and well known to those skilled inthe art to obtain full-length DNAs, or extend short DNAs, for examplethose based on the method of Rapid Amplification of cDNA ends (RACE)(see, for example, Frohman, et al., PNAS USA 85: 8998-9002, 1988).Recent modifications of the technique, exemplified by the Marathon™technology (Clontech Laboratories Inc.) for example, have significantlysimplified the search for longer cDNAs. In the Marathon™ technology,cDNAs have been prepared from mRNA extracted from a chosen tissue and an‘adaptor’ sequence ligated onto each end. Nucleic acid amplification(PCR) is then carried out to amplify the “missing” 5′ end of the DNAusing a combination of gene specific and adaptor specificoligonucleotide primers. The PCR reaction is then repeated using“nested” primers, that is, primers designed to anneal within theamplified product (typically an adaptor specific primer that annealsfurther 3′ in the adaptor sequence and a gene specific primer thatanneals further 5′ in the selected gene sequence). The products of thisreaction can then be analyzed by DNA sequencing and a full-length DNAconstructed either by joining the product directly to the existing DNAto give a complete sequence, or carrying out a separate full-length PCRusing the new sequence information for the design of the 5′ primer.

The polynucleotides and polypeptides of the invention may be employed,for example, as research reagents and materials for discovery oftreatments of and diagnostics for diseases, particularly human diseases,as further discussed herein relating to polynucleotide assays.

The polynucleotides of the invention that are oligonucleotides derivedfrom a sequence of SEQ ID NOS:1 or 3 may be used in the processes hereinas described, but preferably for PCR, to determine whether or not thepolynucleotides identified herein in whole or in part are transcribed inbacteria in infected tissue. It is recognized that such sequences willalso have utility in diagnosis of the stage of infection and type ofinfection the pathogen has attained.

The invention also provides polynucleotides that encode a polypeptidethat is the mature protein plus additional amino or carboxyl-terminalamino acids, or amino acids interior to the mature polypeptide (when themature form has more than one polypeptide chain, for instance). Suchsequences may play a role in processing of a protein from precursor to amature form, may allow protein transport, may lengthen or shortenprotein half-life or may facilitate manipulation of a protein for assayor production, among other things. As generally is the case in vivo, theadditional amino acids may be processed away from the mature protein bycellular enzymes.

For each and every polynucleotide of the invention there is provided apolynucleotide complementary to it. It is preferred that thesecomplementary polynucleotides are fully complementary to eachpolynucleotide with which they are complementary.

A precursor protein, having a mature form of the polypeptide fused toone or more prosequences may be an inactive form of the polypeptide.When prosequences are removed such inactive precursors generally areactivated. Some or all of the prosequences may be removed beforeactivation. Generally, such precursors are called proproteins.

In addition to the standard A, G, C, T/U representations fornucleotides, the term “N” may also be used in describing certainpolynucleotides of the invention. “N” means that any of the four DNA orRNA nucleotides may appear at such a designated position in the DNA orRNA sequence, except it is preferred that N is not a nucleic acid thatwhen taken in combination with adjacent nucleotide positions, when readin the correct reading frame, would have the effect of generating apremature termination codon in such reading frame.

In sum, a polynucleotide of the invention may encode a mature protein, amature protein plus a leader sequence (which may be referred to as apreprotein), a precursor of a mature protein having one or moreprosequences that are not the leader sequences of a preprotein, or apreproprotein, which is a precursor to a proprotein, having a leadersequence and one or more prosequences, which generally are removedduring processing steps that produce active and mature forms of thepolypeptide.

In accordance with an aspect of the invention, there is provided the useof a polynucleotide of the invention for therapeutic or prophylacticpurposes, in particular genetic immunization.

The use of a polynucleotide of the invention in genetic immunizationwill preferably employ a suitable delivery method such as directinjection of plasmid DNA into muscles (Wolff et al., Hum Mol Genet(1992) 1: 363, Manthorpe et al., Hum. Gene Ther. (1983) 4: 419),delivery of DNA complexed with specific protein carriers (Wu et al., JBiol. Chem. (1989) 264: 16985), coprecipitation of DNA with calciumphosphate (Benvenisty & Reshef, PNAS USA, (1986) 83: 9551),encapsulation of DNA in various forms of liposomes (Kaneda et al.,Science (1989) 243: 375), particle bombardment (Tang et al., Nature(1992) 356:152, Eisenbraun et al., DNA Cell Biol (1993) 12: 791) and invivo infection using cloned retroviral vectors (Seeger et al., PNAS USA(1984) 81: 5849).

Vectors, Host Cells, Expression Systems

The invention also relates to vectors that comprise a polynucleotide orpolynucleotides of the invention, host cells that are geneticallyengineered with vectors of the invention and the production ofpolypeptides of the invention by recombinant techniques. Cell-freetranslation systems can also be employed to produce such proteins usingRNAs derived from the DNA constructs of the invention.

Recombinant polypeptides of the present invention may be prepared byprocesses well known in those skilled in the art from geneticallyengineered host cells comprising expression systems. Accordingly, in afurther aspect, the present invention relates to expression systems thatcomprise a polynucleotide or polynucleotides of the present invention,to host cells which are genetically engineered with such expressionsystems, and to the production of polypeptides of the invention byrecombinant techniques.

For recombinant production of the polypeptides of the invention, hostcells can be genetically engineered to incorporate expression systems orportions thereof or polynucleotides of the invention. Introduction of apolynucleotide into the host cell can be effected by methods describedin many standard laboratory manuals, such as Davis, et al., BASICMETHODS IN MOLECULAR BIOLOGY, (1986) and Sambrook, et al., MOLECULARCLONING: A LABORATORY MANUAL, 2nd Ed., Cold Spring Harbor LaboratoryPress, Cold Spring Harbor, N.Y. (1989), such as, calcium phosphatetransfection, DEAE-dextran mediated transfection, transvection,microinjection, cationic lipid-mediated transfection, electroporation,transduction, scrape loading, ballistic introduction and infection.

Representative examples of appropriate hosts include bacterial cells,such as cells of streptococci, staphylococci, enterococci, E. coli,streptomyces, cyanobacteria, Bacillus subtilis, Neisseria meningitidisand Moraxella catarrhalis; fungal cells, such as cells of a yeast,Kluveromyces, Saccharomyces, a basidiomycete, Candida albicans andAspergillus; insect cells such as cells of Drosophila S2 and SpodopteraSf9; animal cells such as CHO, COS, HeLa, C127, 3T3, BHK, 293, CV-1 andBowes melanoma cells; and plant cells, such as cells of a gymnosperm orangiosperm.

A great variety of expression systems can be used to produce thepolypeptides of the invention. Such vectors include, among others,chromosomal-, episomal- and virus-derived vectors, for example, vectorsderived from bacterial plasmids, from bacteriophage, from transposons,from yeast episomes, from insertion elements, from yeast chromosomalelements, from viruses such as baculoviruses, papova viruses, such asSV40, vaccinia viruses, adenoviruses, fowl pox viruses, pseudorabiesviruses, picornaviruses, retroviruses, and alphaviruses and vectorsderived from combinations thereof, such as those derived from plasmidand bacteriophage genetic elements, such as cosmids and phagemids. Theexpression system constructs may contain control regions that regulateas well as engender expression. Generally, any system or vector suitableto maintain, propagate or express polynucleotides and/or to express apolypeptide in a host may be used for expression in this regard. Theappropriate DNA sequence may be inserted into the expression system byany of a variety of well-known and routine techniques, such as, forexample, those set forth in Sambrook et al., MOLECULAR CLONING, ALABORATORY MANUAL, (supra).

In recombinant expression systems in eukaryotes, for secretion of atranslated protein into the lumen of the endoplasmic reticulum, into theperiplasmic space or into the extracellular environment, appropriatesecretion signals may be incorporated into the expressed polypeptide.These signals may be endogenous to the polypeptide or they may beheterologous signals.

Polypeptides of the present invention can be recovered and purified fromrecombinant cell cultures by well-known methods including ammoniumsulfate or ethanol precipitation, acid extraction, anion or cationexchange chromatography, phosphocellulose chromatography, hydrophobicinteraction chromatography, affinity chromatography, hydroxylapatitechromatography and lectin chromatography. Most preferably, ion metalaffinity chromatography (IMAC) is employed for purification. Well knowntechniques for refolding proteins may be employed to regenerate activeconformation when the polypeptide is denatured during intracellularsynthesis, isolation and or purification.

The expression system may also be a recombinant live microorganism, suchas a virus or bacterium. The gene of interest can be inserted into thegenome of a live recombinant virus or bacterium. Inoculation and in vivoinfection with this live vector will lead to in vivo expression of theantigen and induction of immune responses. Viruses and bacteria used forthis purpose are for instance: poxviruses (e.g; vaccinia, fowlpox,canarypox), alphaviruses (Sindbis virus, Semliki Forest Virus,Venezuelian Equine Encephalitis Virus), adenoviruses, adeno-associatedvirus, picornaviruses (poliovirus, rhinovirus), herpesviruses (varicellazoster virus, etc), Listeria, Salmonella, Shigella, BCG. These virusesand bacteria can be virulent, or attenuated in various ways in order toobtain live vaccines. Such live vaccines also form part of theinvention.

Diagnostic, Prognostic, Serotyping and Mutation Assays

This invention is also related to the use of BASB027 polynucleotides andpolypeptides of the invention for use as diagnostic reagents. Detectionof BASB027 polynucleotides and/or polypeptides in a eukaryote,particularly a mammal, and especially a human, will provide a diagnosticmethod for diagnosis of disease, staging of disease or response of aninfectious organism to drugs. Eukaryotes, particularly mammals, andespecially humans, particularly those infected or suspected to beinfected with an organism comprising the BASB027 gene or protein, may bedetected at the nucleic acid or amino acid level by a variety of wellknown techniques as well as by methods provided herein.

Polypeptides and polynucleotides for prognosis, diagnosis or otheranalysis may be obtained from a putatively infected and/or infectedindividual's bodily materials. Polynucleotides from any of thesesources, particularly DNA or RNA, may be used directly for detection ormay be amplified enzymatically by using PCR or any other amplificationtechnique prior to analysis. RNA, particularly mRNA, cDNA and genomicDNA may also be used in the same ways. Using amplification,characterization of the species and strain of infectious or residentorganism present in an individual, may be made by an analysis of thegenotype of a selected polynucleotide of the organism. Deletions andinsertions can be detected by a change in size of the amplified productin comparison to a genotype of a reference sequence selected from arelated organism, preferably a different species of the same genus or adifferent strain of the same species. Point mutations can be identifiedby hybridizing amplified DNA to labeled BASB027 polynucleotidesequences. Perfectly or significantly matched sequences can bedistinguished from imperfectly or more significantly mismatched duplexesby DNase or RNase digestion, for DNA or RNA respectively, or bydetecting differences in melting temperatures or renaturation kinetics.Polynucleotide sequence differences may also be detected by alterationsin the electrophoretic mobility of polynucleotide fragments in gels ascompared to a reference sequence. This may be carried out with orwithout denaturing agents. Polynucleotide differences may also bedetected by direct DNA or RNA sequencing. See, for example, Myers etal., Science, 230: 1242 (1985). Sequence changes at specific locationsalso may be revealed by nuclease protection assays, such as RNase, V1and S1 protection assay or a chemical cleavage method. See, for example,Cotton et al., Proc. Natl. Acad. Sci., USA, 85: 4397-4401 (1985).

In another embodiment, an array of oligonucleotides probes comprisingBASB027 nucleotide sequence or fragments thereof can be constructed toconduct efficient screening of, for example, genetic mutations,serotype, taxonomic classification or identification. Array technologymethods are well known and have general applicability and can be used toaddress a variety of questions in molecular genetics including geneexpression, genetic linkage, and genetic variability (see, for example,Chee et al., Science, 274: 610 (1996)).

Thus in another aspect, the present invention relates to a diagnostickit which comprises:

(a) a polynucleotide of the present invention, preferably the nucleotidesequence of SEQ ID NO:1 or 3, or a fragment thereof;

(b) a nucleotide sequence complementary to that of (a);

(c) a polypeptide of the present invention, preferably the polypeptideof SEQ ID NO:2 or 4 or a fragment thereof; or

(d) an antibody to a polypeptide of the present invention, preferably tothe polypeptide of SEQ ID NO:2 or 4.

It will be appreciated that in any such kit, (a), (b), (c) or (d) maycomprise a substantial component. Such a kit will be of use indiagnosing a disease or susceptibility to a Disease, among others.

This invention also relates to the use of polynucleotides of the presentinvention as diagnostic reagents. Detection of a mutated form of apolynucleotide of the invention, preferably SEQ ID NO:1 or 3, which isassociated with a disease or pathogenicity will provide a diagnostictool that can add to, or define, a diagnosis of a disease, a prognosisof a course of disease, a determination of a stage of disease, or asusceptibility to a disease, which results from under-expression,over-expression or altered expression of the polynucleotide. Organisms,particularly infectious organisms, carrying mutations in suchpolynucleotide may be detected at the polynucleotide level by a varietyof techniques, such as those described elsewhere herein.

Cells from an organism carrying mutations or polymorphisms (allelicvariations) in a polynucleotide and/or polypeptide of the invention mayalso be detected at the polynucleotide or polypeptide level by a varietyof techniques, to allow for serotyping, for example. For example, RT-PCRcan be used to detect mutations in the RNA. It is particularly preferredto use RT-PCR in conjunction with automated detection systems, such as,for example, GeneScan. RNA, cDNA or genomic DNA may also be used for thesame purpose, PCR. As an example, PCR primers complementary to apolynucleotide encoding BASB027 polypeptide can be used to identify andanalyze mutations.

The invention further provides primers with 1, 2, 3 or 4 nucleotidesremoved from the 5′ and/or the 3′ end. These primers may be used for,among other things, amplifying BASB027 DNA and/or RNA isolated from asample derived from an individual, such as a bodily material. Theprimers may be used to amplify a polynucleotide isolated from aninfected individual, such that the polynucleotide may then be subject tovarious techniques for elucidation of the polynucleotide sequence. Inthis way, mutations in the polynucleotide sequence may be detected andused to diagnose and/or prognose the infection or its stage or course,or to serotype and/or classify the infectious agent.

The invention further provides a process for diagnosing, disease,preferably bacterial infections, more preferably infections caused byMoraxella catarrhalis, comprising determining from a sample derived froman individual, such as a bodily material, an increased level ofexpression of polynucleotide having a sequence of SEQ ID NO:1 or 3.Increased or decreased expression of a BASB027 polynucleotide can bemeasured using any on of the methods well known in the art for thequantitation of polynucleotides, such as, for example, amplification,PCR, RT-PCR, RNase protection, Northern blotting, spectrometry and otherhybridization methods.

In addition, a diagnostic assay in accordance with the invention fordetecting over-expression of BASB027 polypeptide compared to normalcontrol tissue samples may be used to detect the presence of aninfection, for example. Assay techniques that can be used to determinelevels of a BASB027 polypeptide, in a sample derived from a host, suchas a bodily material, are well-known to those of skill in the art. Suchassay methods include radioimmunoassays, competitive-binding assays,Western Blot analysis, antibody sandwich assays, antibody detection andELISA assays.

The polynucleotides of the invention may be used as components ofpolynucleotide arrays, preferably high density arrays or grids. Thesehigh density arrays are particularly useful for diagnostic andprognostic purposes. For example, a set of spots each comprising adifferent gene, and further comprising a polynucleotide orpolynucleotides of the invention, may be used for probing, such as usinghybridization or nucleic acid amplification, using a probes obtained orderived from a bodily sample, to determine the presence of a particularpolynucleotide sequence or related sequence in an individual. Such apresence may indicate the presence of a pathogen, particularly Moraxellacatarrhalis, and may be useful in diagnosing and/or prognosing diseaseor a course of disease. A grid comprising a number of variants of thepolynucleotide sequence of SEQ ID NO:1 or 3 are preferred. Alsopreferred is a comprising a number of variants of a polynucleotidesequence encoding the polypeptide sequence of SEQ ID NO:2 or 4.

Antibodies

The polypeptides and polynucleotides of the invention or variantsthereof, or cells expressing the same can be used as immunogens toproduce antibodies immunospecific for such polypeptides orpolynucleotides respectively.

In certain preferred embodiments of the invention there are providedantibodies against BASB027 polypeptides or polynucleotides.

Antibodies generated against the polypeptides or polynucleotides of theinvention can be obtained by administering the polypeptides and/orpolynucleotides of the invention, or epitope-bearing fragments of eitheror both, analogues of either or both, or cells expressing either orboth, to an animal, preferably a nonhuman, using routine protocols. Forpreparation of monoclonal antibodies, any technique known in the artthat provides antibodies produced by continuous cell line cultures canbe used. Examples include various techniques, such as those in Kohler,G. and Milstein, C., Nature 256: 495-497 (1975); Kozbor et al.,Immunology Today 4: 72 (1983); Cole et al., pg. 77-96 in MONOCLONALANTIBODIES AND CANCER THERAPY, Alan R. Liss, Inc. (1985).

Techniques for the production of single chain antibodies (U.S. Pat. No.4,946,778) can be adapted to produce single chain antibodies topolypeptides or polynucleotides of this invention. Also, transgenicmice, or other organisms or animals, such as other mammals, may be usedto express humanized antibodies immunospecific to the polypeptides orpolynucleotides of the invention.

Alternatively, phage display technology may be utilized to selectantibody genes with binding activities towards a polypeptide of theinvention either from repertoires of PCR amplified v-genes oflymphocytes from humans screened for possessing anti-BASB027 or fromnaive libraries (McCafferty, et al., (1990), Nature 348, 552-554; Marks,et al., (1992) Biotechnology 10, 779-783). The affinity of theseantibodies can also be improved by, for example, chain shuffling(Clackson et al., (1991) Nature 352: 628).

The above-described antibodies may be employed to isolate or to identifyclones expressing the polypeptides or polynucleotides of the inventionto purify the polypeptides or polynucleotides by, for example, affinitychromatography.

Thus, among others, antibodies against BASB027-polypeptide orBASB027-polynucleotide may be employed to treat infections, particularlybacterial infections.

Polypeptide variants include antigenically, epitopically orimmunologically equivalent variants form a particular aspect of thisinvention.

Preferably, the antibody or variant thereof is modified to make it lessimmunogenic in the individual. For example, if the individual is humanthe antibody may most preferably be “humanized,” where thecomplimentarity determining region or regions of the hybridoma-derivedantibody has been transplanted into a human monoclonal antibody, forexample as described in Jones et al. (1986), Nature 321, 522-525 orTempest et al., (1991) Biotechnology 9, 266-273.

Antagonists and Agonists—Assays and Molecules

Polypeptides and polynucleotides of the invention may also be used toassess the binding of small molecule substrates and ligands in, forexample, cells, cell-free preparations, chemical libraries, and naturalproduct mixtures. These substrates and ligands may be natural substratesand ligands or may be structural or functional mimetics. See, e.g.,Coligan et al., Current Protocols in Immunology 1(2): Chapter 5 (1991).

The screening methods may simply measure the binding of a candidatecompound to the polypeptide or polynucleotide, or to cells or membranesbearing the polypeptide or polynucleotide, or a fusion protein of thepolypeptide by means of a label directly or indirectly associated withthe candidate compound. Alternatively, the screening method may involvecompetition with a labeled competitor. Further, these screening methodsmay test whether the candidate compound results in a signal generated byactivation or inhibition of the polypeptide or polynucleotide, usingdetection systems appropriate to the cells comprising the polypeptide orpolynucleotide. Inhibitors of activation are generally assayed in thepresence of a known agonist and the effect on activation by the agonistby the presence of the candidate compound is observed. Constitutivelyactive polypeptide and/or constitutively expressed polypeptides andpolynucleotides may be employed in screening methods for inverseagonists or inhibitors, in the absence of an agonist or inhibitor, bytesting whether the candidate compound results in inhibition ofactivation of the polypeptide or polynucleotide, as the case may be.Further, the screening methods may simply comprise the steps of mixing acandidate compound with a solution containing a polypeptide orpolynucleotide of the present invention, to form a mixture, measuringBASB027 polypeptide and/or polynucleotide activity in the mixture, andcomparing the BASB027 polypeptide and/or polynucleotide activity of themixture to a standard. Fusion proteins, such as those made from Fcportion and BASB027 polypeptide, as hereinbefore described, can also beused for high-throughput screening assays to identify antagonists of thepolypeptide of the present invention, as well as of phylogeneticallyand/or functionally related polypeptides (see D. Bennett et al., J. Mol.Recognition, 8:52-58 (1995); and K. Johanson et al., J. Biol. Chem.,270(16):9459-9471 (1995)).

The polynucleotides, polypeptides and antibodies that bind to and/orinteract with a polypeptide of the present invention may also be used toconfigure screening methods for detecting the effect of added compoundson the production of mRNA and/or polypeptide in cells. For example, anELISA assay may be constructed for measuring secreted or cell associatedlevels of polypeptide using monoclonal and polyclonal antibodies bystandard methods known in the art. This can be used to discover agentswhich may inhibit or enhance the production of polypeptide (also calledantagonist or agonist, respectively) from suitably manipulated cells ortissues.

The invention also provides a method of screening compounds to identifythose which enhance (agonist) or block (antagonist) the action ofBASB027 polypeptides or polynucleotides, particularly those compoundsthat are bacteriostatic and/or bactericidal. The method of screening mayinvolve high-throughput techniques. For example, to screen for agonistsor antagonists, a synthetic reaction mix, a cellular compartment, suchas a membrane, cell envelope or cell wall, or a preparation of anythereof, comprising BASB027 polypeptide and a labeled substrate orligand of such polypeptide is incubated in the absence or the presenceof a candidate molecule that may be a BASB027 agonist or antagonist. Theability of the candidate molecule to agonize or antagonize the BASB027polypeptide is reflected in decreased binding of the labeled ligand ordecreased production of product from such substrate. Molecules that bindgratuitously, i.e., without inducing the effects of BASB027 polypeptideare most likely to be good antagonists. Molecules that bind well and, asthe case may be, increase the rate of product production from substrate,increase signal transduction, or increase chemical channel activity areagonists. Detection of the rate or level of, as the case may be,production of product from substrate, signal transduction, or chemicalchannel activity may be enhanced by using a reporter system. Reportersystems that may be useful in this regard include but are not limited tocolorimetric, labeled substrate converted into product, a reporter genethat is responsive to changes in BASB027 polynucleotide or polypeptideactivity, and binding assays known in the art.

Another example of an assay for BASB027 agonists is a competitive assaythat combines BASB027 and a potential agonist with BASB027-bindingmolecules, recombinant BASB027 binding molecules, natural substrates orligands, or substrate or ligand mimetics, under appropriate conditionsfor a competitive inhibition assay. BASB027 can be labeled, such as byradioactivity or a colorimetric compound, such that the number ofBASB027 molecules bound to a binding molecule or converted to productcan be determined accurately to assess the effectiveness of thepotential antagonist.

Potential antagonists include, among others, small organic molecules,peptides, polypeptides and antibodies that bind to a polynucleotideand/or polypeptide of the invention and thereby inhibit or extinguishits activity or expression. Potential antagonists also may be smallorganic molecules, a peptide, a polypeptide such as a closely relatedprotein or antibody that binds the same sites on a binding molecule,such as a binding molecule, without inducing BASB027-induced activities,thereby preventing the action or expression of BASB027 polypeptidesand/or polynucleotides by excluding BASB027 polypeptides and/orpolynucleotides from binding.

Potential antagonists include a small molecule that binds to andoccupies the binding site of the polypeptide thereby preventing bindingto cellular binding molecules, such that normal biological activity isprevented. Examples of small molecules include but are not limited tosmall organic molecules, peptides or peptide-like molecules. Otherpotential antagonists include antisense molecules (see Okano, J.Neurochem. 56: 560 (1991); OLIGODEOXYNUCLEOTIDES AS ANTISENSE INHIBITORSOF GENE EXPRESSION, CRC Press, Boca Raton, Fla. (1988), for adescription of these molecules). Preferred potential antagonists includecompounds related to and variants of BASB027.

In a further aspect, the present invention relates to geneticallyengineered soluble fusion proteins comprising a polypeptide of thepresent invention, or a fragment thereof, and various portions of theconstant regions of heavy or light chains of immunoglobulins of varioussubclasses (IgG, IgM, IgA, IgE). Preferred as an immunoglobulin is theconstant part of the heavy chain of human IgG, particularly IgG1, wherefusion takes place at the hinge region. In a particular embodiment, theFc part can be removed simply by incorporation of a cleavage sequencewhich can be cleaved with blood clotting factor Xa. Furthermore, thisinvention relates to processes for the preparation of these fusionproteins by genetic engineering, and to the use thereof for drugscreening, diagnosis and therapy. A further aspect of the invention alsorelates to polynucleotides encoding such fusion proteins. Examples offusion protein technology can be found in International PatentApplication Nos. WO94/29458 and WO94/22914.

Each of the polynucleotide sequences provided herein may be used in thediscovery and development of antibacterial compounds. The encodedprotein, upon expression, can be used as a target for the screening ofantibacterial drugs. Additionally, the polynucleotide sequences encodingthe amino terminal regions of the encoded protein or Shine-Delgarno orother translation facilitating sequences of the respective mRNA can beused to construct antisense sequences to control the expression of thecoding sequence of interest.

The invention also provides the use of the polypeptide, polynucleotide,agonist or antagonist of the invention to interfere with the initialphysical interaction between a pathogen or pathogens and a eukaryotic,preferably mammalian, host responsible for sequelae of infection. Inparticular, the molecules of the invention may be used: in theprevention of adhesion of bacteria, in particular gram positive and/orgram negative bacteria, to eukaryotic, preferably mammalian,extracellular matrix proteins on in-dwelling devices or to extracellularmatrix proteins in wounds; to block bacterial adhesion betweeneukaryotic, preferably mammalian, extracellular matrix proteins andbacterial BASB027 proteins that mediate tissue damage and/or; to blockthe normal progression of pathogenesis in infections initiated otherthan by the implantation of in-dwelling devices or by other surgicaltechniques.

In accordance with yet another aspect of the invention, there areprovided BASB027 agonists and antagonists, preferably bacteristatic orbactericidal agonists and antagonists.

The antagonists and agonists of the invention may be employed, forinstance, to prevent, inhibit and/or treat diseases.

In a further aspect, the present invention relates to mimotopes of thepolypeptide of the invention. A mimotope is a peptide sequence,sufficiently similar to the native peptide (sequentially orstructurally), which is capable of being recognised by antibodies whichrecognise the native peptide; or is capable of raising antibodies whichrecognise the native peptide when coupled to a suitable carrier.

Peptide mimotopes may be designed for a particular purpose by addition,deletion or substitution of elected amino acids. Thus, the peptides maybe modified for the purposes of ease of conjugation to a proteincarrier. For example, it may be desirable for some chemical conjugationmethods to include a terminal cysteine. In addition it may be desirablefor peptides conjugated to a protein carrier to include a hydrophobicterminus distal from the conjugated terminus of the peptide, such thatthe free unconjugated end of the peptide remains associated with thesurface of the carrier protein. Thereby presenting the peptide in aconformation which most closely resembles that of the peptide as foundin the context of the whole native molecule. For example, the peptidesmay be altered to have an N-terminal cysteine and a C-terminalhydrophobic amidated tail. Alternatively, the addition or substitutionof a D-stereoisomer form of one or more of the amino acids may beperformed to create a beneficial derivative, for example to enhancestability of the peptide.

Alternatively, peptide mimotopes may be identified using antibodieswhich are capable themselves of binding to the polypeptides of thepresent invention using techniques such as phage display technology (EP0 552 267 B1). This technique, generates a large number of peptidesequences which mimic the structure of the native peptides and are,therefore, capable of binding to anti-native peptide antibodies, but maynot necessarily themselves share significant sequence homology to thenative polypeptide.

Vaccines

Another aspect of the invention relates to a method for inducing animmunological response in an individual, particularly a mammal,preferably humans, which comprises inoculating the individual withBASB027 polynucleotide and/or polypeptide, or a fragment or variantthereof, adequate to produce antibody and/or T cell immune response toprotect said individual from infection, particularly bacterial infectionand most particularly Moraxella catarrhalis infection. Also provided aremethods whereby such immunological response slows bacterial replication.Yet another aspect of the invention relates to a method of inducingimmunological response in an individual which comprises delivering tosuch individual a nucleic acid vector, sequence or ribozyme to directexpression of BASB027 polynucleotide and/or polypeptide, or a fragmentor a variant thereof, for expressing BASB027 polynucleotide and/orpolypeptide, or a fragment or a variant thereof in vivo in order toinduce an immunological response, such as, to produce antibody and/or Tcell immune response, including, for example, cytokine-producing T cellsor cytotoxic T cells, to protect said individual, preferably a human,from disease, whether that disease is already established within theindividual or not. One example of administering the gene is byaccelerating it into the desired cells as a coating on particles orotherwise. Such nucleic acid vector may comprise DNA, RNA, a ribozyme, amodified nucleic acid, a DNA/RNA hybrid, a DNA-protein complex or anRNA-protein complex.

A further aspect of the invention relates to an immunologicalcomposition that when introduced into an individual, preferably a human,capable of having induced within it an immunological response, inducesan immunological response in such individual to a BASB027 polynucleotideand/or polypeptide encoded therefrom, wherein the composition comprisesa recombinant BASB027 polynucleotide and/or polypeptide encodedtherefrom and/or comprises DNA and/or RNA which encodes and expresses anantigen of said BASB027 polynucleotide, polypeptide encoded therefrom,or other polypeptide of the invention. The immunological response may beused therapeutically or prophylactically and may take the form ofantibody immunity and/or cellular immunity, such as cellular immunityarising from CTL or CD4+ T cells.

A BASB027 polypeptide or a fragment thereof may be fused with co-proteinor chemical moiety which may or may not by itself produce antibodies,but which is capable of stabilizing the first protein and producing afused or modified protein which will have antigenic and/or immunogenicproperties, and preferably protective properties. Thus fused recombinantprotein, preferably further comprises an antigenic co-protein, such aslipoprotein D from Haemophilus influenzae, Glutathione-S-transferase(GST) or beta-galactosidase, or any other relatively large co-proteinwhich solubilizes the protein and facilitates production andpurification thereof. Moreover, the co-protein may act as an adjuvant inthe sense of providing a generalized stimulation of the immune system ofthe organism receiving the protein. The co-protein may be attached toeither the amino- or carboxy-terminus of the first protein.

Provided by this invention are compositions, particularly vaccinecompositions, and methods comprising the polypeptides and/orpolynucleotides of the invention and immunostimulatory DNA sequences,such as those described in Sato, Y. et al. Science 273: 352 (1996).

Also, provided by this invention are methods using the describedpolynucleotide or particular fragments thereof, which have been shown toencode non-variable regions of bacterial cell surface proteins, inpolynucleotide constructs used in such genetic immunization experimentsin animal models of infection with Moraxella catarrhalis. Suchexperiments will be particularly useful for identifying protein epitopesable to provoke a prophylactic or therapeutic immune response. It isbelieved that this approach will allow for the subsequent preparation ofmonoclonal antibodies of particular value, derived from the requisiteorgan of the animal successfully resisting or clearing infection, forthe development of prophylactic agents or therapeutic treatments ofbacterial infection, particularly Moraxella catarrhalis infection, inmammals, particularly humans.

The invention also includes a vaccine formulation which comprises animmunogenic recombinant polypeptide and/or polynucleotide of theinvention together with a suitable carrier, such as a pharmaceuticallyacceptable carrier. Since the polypeptides and polynucleotides may bebroken down in the stomach, each is preferably administeredparenterally, including, for example, administration that issubcutaneous, intramuscular, intravenous, or intradermal. Formulationssuitable for parenteral administration include aqueous and non-aqueoussterile injection solutions which may contain anti-oxidants, buffers,bacteriostatic compounds and solutes which render the formulationisotonic with the bodily fluid, preferably the blood, of the individual;and aqueous and non-aqueous sterile suspensions which may includesuspending agents or thickening agents. The formulations may bepresented in unit-dose or multi-dose containers, for example, sealedampoules and vials and may be stored in a freeze-dried conditionrequiring only the addition of the sterile liquid carrier immediatelyprior to use.

The vaccine formulation of the invention may also include adjuvantsystems for enhancing the immunogenicity of the formulation. Preferablythe adjuvant system raises preferentially a TH1 type of response.

An immune response may be broadly distinguished into two extremecategories, being a humoral or cell mediated immune responses(traditionally characterised by antibody and cellular effectormechanisms of protection respectively). These categories of responsehave been termed TH1-type responses (cell-mediated response), andTH2-type immune responses (humoral response).

Extreme TH1-type immune responses may be characterised by the generationof antigen specific, haplotype restricted cytotoxic T lymphocytes, andnatural killer cell responses. In mice TH1-type responses are oftencharacterised by the generation of antibodies of the IgG2a subtype,whilst in the human these correspond to IgG1 type antibodies. TH2-typeimmune responses are characterised by the generation of a broad range ofimmunoglobulin isotypes including in mice IgG1, IgA, and IgM.

It can be considered that the driving force behind the development ofthese two types of immune responses are cytokines High levels ofTH1-type cytokines tend to favour the induction of cell mediated immuneresponses to the given antigen, whilst high levels of TH2-type cytokinestend to favour the induction of humoral immune responses to the antigen.

The distinction of TH1 and TH2-type immune responses is not absolute. Inreality an individual will support an immune response which is describedas being predominantly TH1 or predominantly TH2. However, it is oftenconvenient to consider the families of cytokines in terms of thatdescribed in murine CD4+ve T cell clones by Mosmann and Coffman(Mosmann, T. R. and Coffman, R. L. (1989) TH1 and TH2 cells: differentpatterns of lymphokine secretion lead to different functionalproperties. Annual Review of Immunology, 7, p 145-173). Traditionally,TH1-type responses are associated with the production of the INF-γ andIL-2 cytokines by T-lymphocytes. Other cytokines often directlyassociated with the induction of TH1-type immune responses are notproduced by T-cells, such as IL-12. In contrast, TH2-type responses areassociated with the secretion of IL-4, IL-5, IL-6 and IL-13.

It is known that certain vaccine adjuvants are particularly suited tothe stimulation of either TH1 or TH2-type cytokine responses.Traditionally the best indicators of the TH1:TH2 balance of the immuneresponse after a vaccination or infection includes direct measurement ofthe production of TH1 or TH2 cytokines by T lymphocytes in vitro afterrestimulation with antigen, and/or the measurement of the IgG1:IgG2aratio of antigen specific antibody responses.

Thus, a TH1-type adjuvant is one which preferentially stimulatesisolated T-cell populations to produce high levels of TH1-type cytokineswhen re-stimulated with antigen in vitro, and promotes development ofboth CD8+ cytotoxic T lymphocytes and antigen specific immunoglobulinresponses associated with TH1-type isotype.

Adjuvants which are capable of preferential stimulation of the TH1 cellresponse are described in International Patent Application No. WO94/00153 and WO 95/17209.

3 De-O-acylated monophosphoryl lipid A (3D-MPL) is one such adjuvant.This is known from GB 2220211 (Ribi). Chemically it is a mixture of 3De-O-acylated monophosphoryl lipid A with 4, 5 or 6 acylated chains andis manufactured by Ribi Immunochem, Montana. A preferred form of 3De-O-acylated monophosphoryl lipid A is disclosed in European Patent 0689 454 B1 (SmithKline Beecham Biologicals SA).

Preferably, the particles of 3D-MPL are small enough to be sterilefiltered through a 0.22 micron membrane (European Patent number 0 689454).

3D-MPL will be present in the range of 10 μg-100 μg preferably 25-50 μgper dose wherein the antigen will typically be present in a range 2-50μg per dose.

Another preferred adjuvant comprises QS21, an Hplc purified non-toxicfraction derived from the bark of Quillaja Saponaria Molina. Optionallythis may be admixed with 3 De-O-acylated monophosphoryl lipid A(3D-MPL), optionally together with an carrier.

The method of production of QS21 is disclosed in U.S. Pat. No.5,057,540.

Non-reactogenic adjuvant formulations containing QS21 have beendescribed previously (WO 96/33739). Such formulations comprising QS21and cholesterol have been shown to be successful TH1 stimulatingadjuvants when formulated together with an antigen.

Further adjuvants which are preferential stimulators of TH1 cellresponse include immunomodulatory oligonucleotides, for exampleunmethylated CpG sequences as disclosed in WO 96/02555.

Combinations of different TH1 stimulating adjuvants, such as thosementioned hereinabove, are also contemplated as providing an adjuvantwhich is a preferential stimulator of TH1 cell response. For example,QS21 can be formulated together with 3D-MPL. The ratio of QS21:3D-MPLwill typically be in the order of 1:10 to 10:1; preferably 1:5 to 5:1and often substantially 1:1. The preferred range for optimal synergy is2.5:1 to 1:1 3D-MPL: QS21.

Preferably a carrier is also present in the vaccine compositionaccording to the invention. The carrier may be an oil in water emulsion,or an aluminium salt, such as aluminium phosphate or aluminiumhydroxide.

A preferred oil-in-water emulsion comprises a metabolisible oil, such assqualene, alpha tocopherol and Tween 80. In a particularly preferredaspect the antigens in the vaccine composition according to theinvention are combined with QS21 and 3D-MPL in such an emulsion.Additionally the oil in water emulsion may contain span 85 and/orlecithin and/or tricaprylin.

Typically for human administration QS21 and 3D-MPL will be present in avaccine in the range of 1 μg-200 μg, such as 10-100 μg, preferably 10μg-50 μg per dose. Typically the oil in water will comprise from 2 to10% squalene, from 2 to 10% alpha tocopherol and from 0.3 to 3% tween80. Preferably the ratio of squalene: alpha tocopherol is equal to orless than 1 as this provides a more stable emulsion. Span 85 may also bepresent at a level of 1%. In some cases it may be advantageous that thevaccines of the present invention will further contain a stabiliser.

Non-toxic oil in water emulsions preferably contain a non-toxic oil,e.g., squalane or squalene, an emulsifier, e.g., Tween 80, in an aqueouscarrier. The aqueous carrier may be, for example, phosphate bufferedsaline.

A particularly potent adjuvant formulation involving QS21, 3D-MPL andtocopherol in an oil in water emulsion is described in WO 95/17210.

The present invention also provides a polyvalent vaccine compositioncomprising a vaccine formulation of the invention in combination withother antigens, in particular antigens useful for treating cancers,autoimmune diseases and related conditions. Such a polyvalent vaccinecomposition may include a TH-1 inducing adjuvant as hereinbeforedescribed.

While the invention has been described with reference to certain BASB027polypeptides and polynucleotides, it is to be understood that thiscovers fragments of the naturally occurring polypeptides andpolynucleotides, and similar polypeptides and polynucleotides withadditions, deletions or substitutions which do not substantially affectthe immunogenic properties of the recombinant polypeptides orpolynucleotides.

Compositions, Kits and Administration

In a further aspect of the invention there are provided compositionscomprising a BASB027 polynucleotide and/or a BASB027 polypeptide foradministration to a cell or to a multicellular organism.

The invention also relates to compositions comprising a polynucleotideand/or a polypeptides discussed herein or their agonists or antagonists.The polypeptides and polynucleotides of the invention may be employed incombination with a non-sterile or sterile carrier or carriers for usewith cells, tissues or organisms, such as a pharmaceutical carriersuitable for administration to an individual. Such compositionscomprise, for instance, a media additive or a therapeutically effectiveamount of a polypeptide and/or polynucleotide of the invention and apharmaceutically acceptable carrier or excipient. Such carriers mayinclude, but are not limited to, saline, buffered saline, dextrose,water, glycerol, ethanol and combinations thereof. The formulationshould suit the mode of administration. The invention further relates todiagnostic and pharmaceutical packs and kits comprising one or morecontainers filled with one or more of the ingredients of theaforementioned compositions of the invention.

Polypeptides, polynucleotides and other compounds of the invention maybe employed alone or in conjunction with other compounds, such astherapeutic compounds.

The pharmaceutical compositions may be administered in any effective,convenient manner including, for instance, administration by topical,oral, anal, vaginal, intravenous, intraperitoneal, intramuscular,subcutaneous, intranasal or intradermal routes among others.

In therapy or as a prophylactic, the active agent may be administered toan individual as an injectable composition, for example as a sterileaqueous dispersion, preferably isotonic.

In a further aspect, the present invention provides for pharmaceuticalcompositions comprising a therapeutically effective amount of apolypeptide and/or polynucleotide, such as the soluble form of apolypeptide and/or polynucleotide of the present invention, agonist orantagonist peptide or small molecule compound, in combination with apharmaceutically acceptable carrier or excipient. Such carriers include,but are not limited to, saline, buffered saline, dextrose, water,glycerol, ethanol, and combinations thereof. The invention furtherrelates to pharmaceutical packs and kits comprising one or morecontainers filled with one or more of the ingredients of theaforementioned compositions of the invention. Polypeptides,polynucleotides and other compounds of the present invention may beemployed alone or in conjunction with other compounds, such astherapeutic compounds.

The composition will be adapted to the route of administration, forinstance by a systemic or an oral route. Preferred forms of systemicadministration include injection, typically by intravenous injection.Other injection routes, such as subcutaneous, intramuscular, orintraperitoneal, can be used. Alternative means for systemicadministration include transmucosal and transdermal administration usingpenetrants such as bile salts or fusidic acids or other detergents. Inaddition, if a polypeptide or other compounds of the present inventioncan be formulated in an enteric or an encapsulated formulation, oraladministration may also be possible. Administration of these compoundsmay also be topical and/or localized, in the form of salves, pastes,gels, solutions, powders and the like.

For administration to mammals, and particularly humans, it is expectedthat the daily dosage level of the active agent will be from 0.01 mg/kgto 10 mg/kg, typically around 1 mg/kg. The physician in any event willdetermine the actual dosage which will be most suitable for anindividual and will vary with the age, weight and response of theparticular individual. The above dosages are exemplary of the averagecase. There can, of course, be individual instances where higher orlower dosage ranges are merited, and such are within the scope of thisinvention.

The dosage range required depends on the choice of peptide, the route ofadministration, the nature of the formulation, the nature of thesubject's condition, and the judgment of the attending practitioner.Suitable dosages, however, are in the range of 0.1-100 μg/kg of subject.

A vaccine composition is conveniently in injectable form. Conventionaladjuvants may be employed to enhance the immune response. A suitableunit dose for vaccination is 0.5-5 microgram/kg of antigen, and suchdose is preferably administered 1-3 times and with an interval of 1-3weeks. With the indicated dose range, no adverse toxicological effectswill be observed with the compounds of the invention which wouldpreclude their administration to suitable individuals.

Wide variations in the needed dosage, however, are to be expected inview of the variety of compounds available and the differingefficiencies of various routes of administration. For example, oraladministration would be expected to require higher dosages thanadministration by intravenous injection. Variations in these dosagelevels can be adjusted using standard empirical routines foroptimization, as is well understood in the art.

Sequence Databases, Sequences in a Tangible Medium, and Algorithms

Polynucleotide and polypeptide sequences form a valuable informationresource with which to determine their 2- and 3-dimensional structuresas well as to identify further sequences of similar homology. Theseapproaches are most easily facilitated by storing the sequence in acomputer readable medium and then using the stored data in a knownmacromolecular structure program or to search a sequence database usingwell known searching tools, such as the GCG program package.

Also provided by the invention are methods for the analysis of charactersequences or strings, particularly genetic sequences or encoded proteinsequences. Preferred methods of sequence analysis include, for example,methods of sequence homology analysis, such as identity and similarityanalysis, DNA, RNA and protein structure analysis, sequence assembly,cladistic analysis, sequence motif analysis, open reading framedetermination, nucleic acid base calling, codon usage analysis, nucleicacid base trimming, and sequencing chromatogram peak analysis.

A computer based method is provided for performing homologyidentification. This method comprises the steps of: providing a firstpolynucleotide sequence comprising the sequence of a polynucleotide ofthe invention in a computer readable medium; and comparing said firstpolynucleotide sequence to at least one second polynucleotide orpolypeptide sequence to identify homology.

A computer based method is also provided for performing homologyidentification, said method comprising the steps of: providing a firstpolypeptide sequence comprising the sequence of a polypeptide of theinvention in a computer readable medium; and comparing said firstpolypeptide sequence to at least one second polynucleotide orpolypeptide sequence to identify homology.

All publications and references, including but not limited to patentsand patent applications, cited in this specification are hereinincorporated by reference in their entirety as if each individualpublication or reference were specifically and individually indicated tobe incorporated by reference herein as being fully set forth. Any patentapplication to which this application claims priority is alsoincorporated by reference herein in its entirety in the manner describedabove for publications and references.

DEFINITIONS

“Identity,” as known in the art, is a relationship between two or morepolypeptide sequences or two or more polynucleotide sequences, as thecase may be, as determined by comparing the sequences. In the art,“identity” also means the degree of sequence relatedness betweenpolypeptide or polynucleotide sequences, as the case may be, asdetermined by the match between strings of such sequences. “Identity”can be readily calculated by known methods, including but not limited tothose described in (Computational Molecular Biology, Lesk, A. M., ed.,Oxford University Press, New York, 1988; Biocomputing: Informatics andGenome Projects, Smith, D. W., ed., Academic Press, New York, 1993;Computer Analysis of Sequence Data, Part I, Griffin, A. M., and Griffin,H. G., eds., Humana Press, New Jersey, 1994; Sequence Analysis inMolecular Biology, von Heine, G., Academic Press, 1987; and SequenceAnalysis Primer, Gribskov, M. and Devereux, J., eds., M Stockton Press,New York, 1991; and Carillo, H., and Lipman, D., SIAM J. Applied Math.,48: 1073 (1988). Methods to determine identity are designed to give thelargest match between the sequences tested. Moreover, methods todetermine identity are codified in publicly available computer programs.Computer program methods to determine identity between two sequencesinclude, but are not limited to, the GAP program in the GCG programpackage (Devereux, J., et al., Nucleic Acids Research 12(1): 387(1984)), BLASTP, BLASTN (Altschul, S. F. et al., J. Molec. Biol. 215:403-410 (1990), and FASTA (Pearson and Lipman Proc. Natl. Acad. Sci. USA85; 2444-2448 (1988). The BLAST family of programs is publicly availablefrom NCBI and other sources (BLAST Manual, Altschul, S., et al., NCBINLM NIH Bethesda, Md. 20894; Altschul, S., et al., J. Mol. Biol. 215:403-410 (1990). The well known Smith Waterman algorithm may also be usedto determine identity.

Parameters for polypeptide sequence comparison include the following:Algorithm: Needleman and Wunsch, J. Mol. Biol. 48: 443-453 (1970)Comparison matrix: BLOSSUM62 from Henikoff and Henikoff,Proc. Natl. Acad. Sci. USA. 89:10915-10919 (1992)

Gap Penalty: 8 Gap Length Penalty: 2

A program useful with these parameters is publicly available as the“gap” program from Genetics Computer Group, Madison Wis. Theaforementioned parameters are the default parameters for peptidecomparisons (along with no penalty for end gaps).Parameters for polynucleotide comparison include the following:Algorithm: Needleman and Wunsch, J. Mol. Biol. 48: 443-453 (1970)Comparison matrix: matches=+10, mismatch=0

Gap Penalty: 50 Gap Length Penalty: 3

Available as: The “gap” program from Genetics Computer Group, MadisonWis. These are the default parameters for nucleic acid comparisons.

A preferred meaning for “identity” for polynucleotides and polypeptides,as the case may be, are provided in (1) and (2) below.

(1) Polynucleotide embodiments further include an isolatedpolynucleotide comprising a polynucleotide sequence having at least a50, 60, 70, 80, 85, 90, 95, 97 or 100% identity to the referencesequence of SEQ ID NO:1, wherein said polynucleotide sequence may beidentical to the reference sequence of SEQ ID NO:1 or may include up toa certain integer number of nucleotide alterations as compared to thereference sequence, wherein said alterations are selected from the groupconsisting of at least one nucleotide deletion, substitution, includingtransition and transversion, or insertion, and wherein said alterationsmay occur at the 5′ or 3′ terminal positions of the reference nucleotidesequence or anywhere between those terminal positions, interspersedeither individually among the nucleotides in the reference sequence orin one or more contiguous groups within the reference sequence, andwherein said number of nucleotide alterations is determined bymultiplying the total number of nucleotides in SEQ ID NO:1 by theinteger defining the percent identity divided by 100 and thensubtracting that product from said total number of nucleotides in SEQ IDNO:1, or:

n _(n) ≦x _(n)−(x _(n) •y),

wherein n_(n) is the number of nucleotide alterations, x_(n) is thetotal number of nucleotides in SEQ ID NO:1, y is 0.50 for 50%, 0.60 for60%, 0.70 for 70%, 0.80 for 80%, 0.85 for 85%, 0.90 for 90%, 0.95 for95%, 0.97 for 97% or 1.00 for 100%, and • is the symbol for themultiplication operator, and wherein any non-integer product of x_(n)and y is rounded down to the nearest integer prior to subtracting itfrom x_(n). Alterations of a polynucleotide sequence encoding thepolypeptide of SEQ ID NO:2 may create nonsense, missense or frameshiftmutations in this coding sequence and thereby alter the polypeptideencoded by the polynucleotide following such alterations.

By way of example, a polynucleotide sequence of the present inventionmay be identical to the reference sequence of SEQ ID NO:1, that is itmay be 100% identical, or it may include up to a certain integer numberof nucleic acid alterations as compared to the reference sequence suchthat the percent identity is less than 100% identity. Such alterationsare selected from the group consisting of at least one nucleic aciddeletion, substitution, including transition and transversion, orinsertion, and wherein said alterations may occur at the 5′ or 3′terminal positions of the reference polynucleotide sequence or anywherebetween those terminal positions, interspersed either individually amongthe nucleic acids in the reference sequence or in one or more contiguousgroups within the reference sequence. The number of nucleic acidalterations for a given percent identity is determined by multiplyingthe total number of nucleic acids in SEQ ID NO:1 by the integer definingthe percent identity divided by 100 and then subtracting that productfrom said total number of nucleic acids in SEQ ID NO:1, or:

n _(n) ≦x _(n)−(x _(n) •y),

wherein n_(n) is the number of nucleic acid alterations, x_(n) is thetotal number of nucleic acids in SEQ ID NO:1, y is, for instance 0.70for 70%, 0.80 for 80%, 0.85 for 85% etc., • is the symbol for themultiplication operator, and wherein any non-integer product of x_(n)and y is rounded down to the nearest integer prior to subtracting itfrom x_(n).

(2) Polypeptide embodiments further include an isolated polypeptidecomprising a polypeptide having at least a 50, 60, 70, 80, 85, 90, 95,97 or 100% identity to a polypeptide reference sequence of SEQ ID NO:2,wherein said polypeptide sequence may be identical to the referencesequence of SEQ ID NO:2 or may include up to a certain integer number ofamino acid alterations as compared to the reference sequence, whereinsaid alterations are selected from the group consisting of at least oneamino acid deletion, substitution, including conservative andnon-conservative substitution, or insertion, and wherein saidalterations may occur at the amino- or carboxy-terminal positions of thereference polypeptide sequence or anywhere between those terminalpositions, interspersed either individually among the amino acids in thereference sequence or in one or more contiguous groups within thereference sequence, and wherein said number of amino acid alterations isdetermined by multiplying the total number of amino acids in SEQ ID NO:2by the integer defining the percent identity divided by 100 and thensubtracting that product from said total number of amino acids in SEQ IDNO:2, or:

n _(a) ≦x _(a)−(x _(a) •y),

wherein n_(a) is the number of amino acid alterations, x_(a) is thetotal number of amino acids in SEQ ID NO:2, y is 0.50 for 50%, 0.60 for60%, 0.70 for 70%, 0.80 for 80%, 0.85 for 85%, 0.90 for 90%, 0.95 for95%, 0.97 for 97% or 1.00 for 100%, and • is the symbol for themultiplication operator, and wherein any non-integer product of x_(a)and y is rounded down to the nearest integer prior to subtracting itfrom x_(a).

By way of example, a polypeptide sequence of the present invention maybe identical to the reference sequence of SEQ ID NO:2, that is it may be100% identical, or it may include up to a certain integer number ofamino acid alterations as compared to the reference sequence such thatthe percent identity is less than 100% identity. Such alterations areselected from the group consisting of at least one amino acid deletion,substitution, including conservative and non-conservative substitution,or insertion, and wherein said alterations may occur at the amino- orcarboxy-terminal positions of the reference polypeptide sequence oranywhere between those terminal positions, interspersed eitherindividually among the amino acids in the reference sequence or in oneor more contiguous groups within the reference sequence. The number ofamino acid alterations for a given % identity is determined bymultiplying the total number of amino acids in SEQ ID NO:2 by theinteger defining the percent identity divided by 100 and thensubtracting that product from said total number of amino acids in SEQ IDNO:2, or:

n _(a) ≦x _(a)−(x _(a) •y),

wherein n_(a) is the number of amino acid alterations, x_(a) is thetotal number of amino acids in SEQ ID NO:2, y is, for instance 0.70 for70%, 0.80 for 80%, 0.85 for 85% etc., and • is the symbol for themultiplication operator, and wherein any non-integer product of x_(a)and y is rounded down to the nearest integer prior to subtracting itfrom x_(a).

“Individual(s),” when used herein with reference to an organism, means amulticellular eukaryote, including, but not limited to a metazoan, amammal, an ovid, a bovid, a simian, a primate, and a human.

“Isolated” means altered “by the hand of man” from its natural state,i.e., if it occurs in nature, it has been changed or removed from itsoriginal environment, or both. For example, a polynucleotide or apolypeptide naturally present in a living organism is not “isolated,”but the same polynucleotide or polypeptide separated from the coexistingmaterials of its natural state is “isolated”, as the term is employedherein. Moreover, a polynucleotide or polypeptide that is introducedinto an organism by transformation, genetic manipulation or by any otherrecombinant method is “isolated” even if it is still present in saidorganism, which organism may be living or non-living.

“Polynucleotide(s)” generally refers to any polyribonucleotide orpolydeoxyribonucleotide, which may be unmodified RNA or DNA or modifiedRNA or DNA including single and double-stranded regions.

“Variant” refers to a polynucleotide or polypeptide that differs from areference polynucleotide or polypeptide, but retains essentialproperties. A typical variant of a polynucleotide differs in nucleotidesequence from another, reference polynucleotide. Changes in thenucleotide sequence of the variant may or may not alter the amino acidsequence of a polypeptide encoded by the reference polynucleotide.Nucleotide changes may result in amino acid substitutions, additions,deletions, fusions and truncations in the polypeptide encoded by thereference sequence, as discussed below. A typical variant of apolypeptide differs in amino acid sequence from another, referencepolypeptide. Generally, differences are limited so that the sequences ofthe reference polypeptide and the variant are closely similar overalland, in many regions, identical. A variant and reference polypeptide maydiffer in amino acid sequence by one or more substitutions, additions,deletions in any combination. A substituted or inserted amino acidresidue may or may not be one encoded by the genetic code. A variant ofa polynucleotide or polypeptide may be a naturally occurring such as anallelic variant, or it may be a variant that is not known to occurnaturally. Non-naturally occurring variants of polynucleotides andpolypeptides may be made by mutagenesis techniques or by directsynthesis.

“Disease(s)” means any disease caused by or related to infection by abacteria, including, for example, otitis media in infants and children,pneumonia in elderlies, sinusitis, nosocomial infections and invasivediseases, chronic otitis media with hearing loss, fluid accumulation inthe middle ear, auditive nerve damage, delayed speech learning,infection of the upper respiratory tract and inflammation of the middleear.

EXAMPLES

The examples below are carried out using standard techniques, which arewell known and routine to those of skill in the art, except whereotherwise described in detail. The examples are illustrative, but do notlimit the invention.

Example 1 Discovery and Confirmatory DNA Sequencing of the BASB027 Genefrom Moraxella catarrhalis Strain ATCC 43617

The BASB027 gene of SEQ ID NO:1 was first discovered in the IncytePathoSeq data base containing unfinished genomic DNA sequences of theMoraxella catarrhalis strain ATCC 43617 (also referred to as strainMc2931). The translation of the BASB027 polynucleotide sequence, shownin SEQ ID NO:2, showed significant similarity (32% identity in a 817amino acids overlap) to the OMP85 outer membrane protein of Neisseriameningitidis.

The sequence of the BASB027 gene was further confirmed experimentally.For this purpose, genomic DNA was extracted from 10¹⁰ cells of the M.catarrhalis cells (strain ATCC 43617) using the QIAGEN genomic DNAextraction kit (Qiagen Gmbh), and 1 μg of this material was submitted toPolymerase Chain Reaction DNA amplification using primers E515515(5′-ACT-ATA-GGG-CAC-GCG-TG-3′) [SEQ ID NO:5] and E515528:(5′-CCT-GCG-TTT-GTT-TGA-TTG-AG-3′) [SEQ ID NO:6]. This PCR product waspurified on a Biorobot 9600 (Qiagen Gmbh) apparatus and subjected to DNAsequencing using the Big Dye Cycle Sequencing kit (Perkin-Elmer) and anABI 377/PRISM DNA sequencer. DNA sequencing was performed on bothstrands with a redundancy of 2 and the full length sequence wasassembled using the SeqMan program from the DNASTAR Lasergene softwarepackage. The resulting DNA sequence and deduced polypeptide sequence areshown as SEQ ID NO:3 and SEQ ID NO:4 respectively. Four nucleotidedifferences distinguish SEQ ID NO:3 from SEQ ID NO:1. Using the MEGALIGNprogram from the DNASTAR Lasergene software package, an alignment of thepolynucleotide sequences of SEQ ID NO:1 and 3 was performed, and isdisplayed in FIG. 2; their level of identity was calculated to be 99.8%.

Using the same program, an alignment of the polypeptide sequences of SEQID NO:2 and 4 was performed, and is displayed in FIG. 3; their level ofidentity was calculated to be 99.8%.

Example 2 Variability Analysis of the BASB027 Gene Among SeveralMoraxella catarrhalis Strains 2A: Restriction Fragment Length Analysis(RFLP).

Genomic DNA was extracted from 16 M. catarrhalis strains (presented inTable 1) as described below. M. catarrhalis was streaked for singlecolonies on BHI agar plates and grown overnight at 37° C. Three or foursingle colonies were picked and used to inoculate a ˜1.5 ml BHI(Brain-heart infusion) broth seed culture which was grown overnight in ashaking incubator, ˜300 rpm, at 37° C. A 500 ml erlenmeyer flaskcontaining ˜150 ml of BHI broth was inoculated with the seed culture andgrown for ˜12-16 hours at 37° C. in a shaking incubator, ˜175 rpm, togenerate cell mass for DNA isolation. Cells were collected bycentrifugation in a Sorvall GSA rotor at ˜2000× g for 15 minutes at roomtemperature. The supernatant was removed and the cell pellet suspendedin ˜5.0 ml of sterile water. An equal volume of lysis buffer (200 mMNaCl, 20 mM EDTA, 40 mM Tris-HCl, pH 8.0, 0.5% (w/v) SDS, 0.5% (v/v)2-mercaptoethanol, and 250 μg/ml of proteinase K) was added and thecells suspended by gentle agitation and trituration. The cell suspensionwas then incubated ˜12 hours at 50° C. to lyse the bacteria and liberatechromosomal DNA. Proteinaceous material was precipitated by the additionof 5.0 ml of saturated NaCl (˜6.0 M, in sterile water) andcentrifugation at ˜5,500× g in a Sorvall SS34 rotor at room temperature.Chromosomal DNA was precipitated from the cleared supernatant by theaddition of two volumes of 100% ethanol. Aggregated DNA was collectedand washed using gentle agitation in a small volume of a 70% ethanolsolution. Purified chromosomal DNA was suspended in sterile water andallowed to dissolve/disburse overnight at 4° C. by gentle rocking. Theconcentration of dissolved DNA was determined spectrophotometrically at260 nm using an extinction coefficient of 1.0 O.D. unit ˜50 μg/ml.

This material was next submitted to PCR amplification using theMC-D15-BamF (5′-AAG GGC CCA ATT ACG CAG AGG GGA TCC ACA GGA CTA CAG CGAGTG ACC ATT GAA AGC TTA C-3′) [SEQ ID NO:7] and MC-D15-SalRC (AAG GGCCCA ATT ACG CAG AGG GTC GAC TTA TTA AAA GAC ACT ACC AAT CTG GAA CTG TACCGT ATC G-3′) [SEQ ID NO:8] oligonucleotides. The corresponding BASB027gene amplicons were then subjected independently to hydrolysis usingrestriction enzymes (AciI, HindIII, MaeIII, NlaIII, RsaI, Sau3AI) andrestriction products were separated by agarose or polyacrylamide gelelectrophoresis using standard molecular biology procedures as describedin “Molecular Cloning, a Laboratory Manual, Second Edition, Eds:Sambrook, Fritsch & Maniatis, Cold Spring Harbor press 1989”. Thephotographs of the resulting electrophoresis gels are displayed inFIG. 1. For each strain, RFLP patterns corresponding to the 6restriction enzymes were scored and combined. Groups of strains sharingidentical combination of RFLP patterns were then defined. Using thismethodology, the strains tested in this study fell into 4 genomic groups(Group 1: Mc2906, Mc 2908, Mc2912, Mc2926; Group 2: Mc2905, Mc2907,Mc2909, Mc2911, Mc2913, Mc2960, Mc2975; Group 3: Mc2910, Mc2912, Mc2956,Mc2969; Group 4: Mc2931). These data support that the Moraxellacatarrhalis population used in this study displays limited nucleotidesequence diversity for the BASB027 gene.

TABLE 1 Features of the Moraxella catarrhalis strains used in this studyStrain Isolated in: from: Mc2904 USA Tympanocentesis Mc2905 USATympanocentesis Mc2906 USA Tympanocentesis Mc2907 USA TympanocentesisMc2908 USA Acute otitis Tympanocentesis Mc2909 USA TympanocentesisMc2910 USA Tympanocentesis Mc2911 USA Acute otitis TympanocentesisMc2912 USA Acute otitis Tympanocentesis Mc2913 USA Acute otitisTympanocentesis Mc2926 USA Tympanocentesis Mc2931/ USA Transtrachealaspirate ATCC 43617 Mc2956 Finland Middle ear fluid Mc2960 FinlandMiddle ear fluid Mc2969 Norway Nasopharynx (Pharyngitis- Rhinitis)Mc2975 Norway Nasopharynx (Rhinitis)

Example 3 Construction of Plasmid to Express Recombinant BASB027 A:Cloning of BASB027.

The BamHI and SalI restriction sites engineered into the forward ([SEQID NO:7]) and reverse complementary ([SEQ ID NO:8]) amplificationprimers, respectively, permitted directional cloning of an ˜2500 by PCRproduct into the commercially available E. coli expression plasmid pQE30(QIAGEN, ampicillin resistant) such that a mature BASB027 protein couldbe expressed as a fusion protein containing a (His)6 affinitychromatography tag at the N-terminus. The BASB027 PCR product waspurified from the amplification reaction using silica gel-based spincolumns (QIAGEN) according to the manufacturers instructions. To producethe required BamHI and SalI termini necessary for cloning, purified PCRproduct was sequentially digested to completion with BamHI and SalIrestriction enzymes as recommended by the manufacturer (LifeTechnologies). Following the first restriction digestion, the PCRproduct was purified via spin column as above to remove salts and elutedin sterile water prior to the second enzyme digestion. The digested DNAfragment was again purified using silica gel-based spin columns prior toligation with the pQE30 plasmid.

B: Production of Expression Vector.

To prepare the expression plasmid pQE30 for ligation, it was similarlydigested to completion with both BamHI and SalI and then treated withcalf intestinal phosphatase (CIP, ˜0.02 units/pmole of 5′ end, LifeTechnologies) as directed by the manufacturer to prevent self ligation.An approximately 5-fold molar excess of the digested fragment to theprepared vector was used to program the ligation reaction. A standard˜20 μl ligation reaction (˜16° C., ˜16 hours), using methods well knownin the art, was performed using T4 DNA ligase (˜2.0 units/reaction, LifeTechnologies). An aliquot of the ligation (˜5 μl) was used to transformelectro-competent M15(pREP4) cells according to methods well known inthe art. Following a ˜2-3 hour outgrowth period at 37° C. in ˜1.0 ml ofLB broth, transformed cells were plated on LB agar plates containingkanamycin (50 μg/ml) and ampicillin (100 μg/ml). Both antibiotics wereincluded in the selection media to ensure that all transformed cellscarried both the pREP4 plasmid (KnR), which carries the lacIq genenecessary for the repression of expression for IPTG-inducible expressionof proteins on pQE30, and the pQE30-BASB027 plasmid (ApR). Plates wereincubated overnight at 37° C. for ˜16 hours. Individual KnR/ApR colonieswere picked with sterile toothpicks and used to “patch” inoculate freshLB KnR/ApR plates as well as a ˜1.0 ml LB KnR/ApR broth culture. Boththe patch plates and the broth culture were incubated overnight at 37°C. in either a standard incubator (plates) or a shaking water bath.

A whole cell-based PCR analysis was employed to verify thattransformants contained the BASB027 DNA insert. Here, the ˜1.0 mlovernight LB Kn/Ap broth culture was transferred to a 1.5 mlpolypropylene tube and the cells collected by centrifugation in aBeckmann microcentrifuge (˜3 min., room temperature, 12,000×g). The cellpellet was suspended in ˜200 μl of sterile water and a ˜10 μl aliquotused to program a ˜50 μl final volume PCR reaction containing bothBASB027 forward and reverse amplification primers. Final concentrationsof the PCR reaction components were essentially the same as thosespecified in example 2 except ˜5.0 units of Taq polymerase was used. Theinitial 95° C. denaturation step was increased to 3 minutes to ensurethermal disruption of the bacterial cells and liberation of plasmid DNA.An ABI Model 9700 thermal cycler and a 32 cycle, three-step thermalamplification profile, i.e. 95° C., 45 sec; 55-58° C., 45 sec, 72° C., 1min., were used to amplify the BASB027 PCR fragment from the lysedtransformant samples. Following thermal amplification, a ˜20 μl aliquotof the reaction was analyzed by agarose gel electrophoresis (0.8%agarose in a Tris-acetate-EDTA (TAE) buffer). DNA fragments werevisualized by UV illumination after gel electrophoresis and ethidiumbromide staining A DNA molecular size standard (1 Kb ladder, LifeTechnologies) was electrophoresed in parallel with the test samples andwas used to estimate the size of the PCR products. Transformants thatproduced the expected ˜2500 by PCR product were identified as strainscontaining a BASB027 expression construct. Expression plasmid containingstrains were then analyzed for the inducible expression of recombinantBASB027.

C: Expression Analysis of PCR-Positive Transformants.

For each PCR-positive transformant identified above, ˜5.0 ml of LB brothcontaining kanamycin (50 μg/ml) and ampicillin (100 μg/ml) wasinoculated with cells from the patch plate and grown overnight at 37° C.with shaking (˜250 rpm). An aliquot of the overnight seed culture (˜1.0ml) was inoculated into a 125 ml erlenmeyer flask containing ˜25 ml ofLB Kn/Ap broth and grown at 37° C. with shaking (˜250 rpm) until theculture turbidity reached O.D.600 of ˜0.5, i.e. mid-log phase (usuallyabout 1.5-2.0 hours). At this time approximately half of the culture(˜12.5 ml) was transferred to a second 125 ml flask and expression ofrecombinant BASB027 protein induced by the addition of IPTG (1.0 M stockprepared in sterile water, Sigma) to a final concentration of 1.0 mM.Incubation of both the IPTG-induced and non-induced cultures continuedfor an additional ˜4 hours at 37° C. with shaking Samples (˜1.0 ml) ofboth induced and non-induced cultures were removed after the inductionperiod and the cells collected by centrifugation in a microcentrifuge atroom temperature for ˜3 minutes. Individual cell pellets were suspendedin ˜50 μl of sterile water, then mixed with an equal volume of 2×Laemelli SDS-PAGE sample buffer containing 2-mercaptoethanol, and placedin boiling water bath for ˜3 min to denature protein. Equal volumes (˜15μl) of both the crude IPTG-induced and the non-induced cell lysates wereloaded onto duplicate 12% Tris/glycine polyacrylamide gel (1 mm thickMini-gels, Novex). The induced and non-induced lysate samples wereelectrophoresed together with prestained molecular weight markers (SeeBlue, Novex) under conventional conditions using a standardSDS/Tris/glycine running buffer (BioRad). Following electrophoresis, onegel was stained with commassie brilliant blue 8250 (BioRad) and thendestained to visualize novel BASB027 IPTG-inducible protein(s). Thesecond gel was electroblotted onto a PVDF membrane (0.45 micron poresize, Novex) for ˜2 hrs at 4° C. using a BioRad Mini-Protean II blottingapparatus and Towbin's methanol (20%) transfer buffer. Blocking of themembrane and antibody incubations were performed according to methodswell known in the art. A monoclonal anti-RGS (His)3 antibody, followedby a second rabbit anti-mouse antibody conjugated to HRP (QIAGEN), wasused to confirm the expression and identity of the BASB027 recombinantprotein. Visualization of the anti-His antibody reactive pattern wasachieved using either an ABT insoluble substrate or using Hyperfilm withthe Amersham ECL chemiluminescence system.

D: Sequence Confirmation.

To further verify that the IPTG-inducible recombinant BASB027 proteinbeing expressed is in the correct open reading frame and not a spuriousmolecule arising from a cloning artifact (i.e. a frame-shift), the DNAsequence of the cloned insert was determined. The DNA sequence for theM. catarrhalis BASB027 gene was obtained from one strand usingconventional asymmetric PCR cycle sequencing methodologies (ABI PrismDye-Terminator Cycle Sequencing, Perkin-Elmer). Sequencing reactionswere programmed with undigested expression plasmid DNA (0.5 μg/r×n) as atemplate and appropriate pQE30 vector-specific and ORF-specificsequencing primers (˜3.5 μmol/rxn). In addition to the template andsequencing primer, each sequencing reaction (˜20 μl) contained the fourdifferent dNTPs (i.e., A, G, C, and T) and the four corresponding ddNTPs(i.e., ddA, ddG, ddC, and ddT) terminator nucleotides; with eachterminator being conjugated to one of the four fluorescent dyes, Joe,Tam, Rox, or Fam. Single strand sequencing elongation products wereterminated at random positions along the template by the incorporationof the dye-labelled ddNTP terminators. Fluorescent dye-labelledtermination products were purified using microcentrifuge size-exclusionchromatography columns (Princeton Genetics), dried under vacuum,suspended in a Template Resuspension Buffer (Perkin-Elmer) for capillaryelectrophoresis or deionized formamide for PAGE, denatured at 95° C. for˜5 min, and analyzed by high resolution capillary electrophoresis (ABI310 Automated DNA Sequenator, Perkin-Elmer) or high resolution PAGE (ABI377 Automated DNA Sequenator) as recommended by the manufacturer. DNAsequence data produced from individual reactions were collected and therelative fluorescent peak intensities analyzed automatically on aPowerMAC computer using ABI Sequence Analysis Software (Perkin-Elmer).Individually autoanalyzed DNA sequences were edited manually foraccuracy before being merged into a consensus single strand sequence“string” using AutoAssembler software (Perkin-Elmer). Sequencingdetermined that the expression plasmid contained the correct sequence inthe correct open reading frame.

Example 4 Production of Recombinant BASB027 Bacterial Strain

A recombinant expression strain of E. coli M15 (pREP4) containing aplasmid (pQE30) encoding BASB027 from M. catarrhalis. was used toproduce cell mass for purification of recombinant protein. Theexpression strain was cultivated on LB agar plates containing 50 μg/mlkanamycin (“Kn”) and 100 μg/ml ampicillin (“Ap”) to ensure both thepREP4 lacIq control plasmid and the pQE30-BASB027 expression constructwere both maintained. For cryopreservation at −80° C., the strain waspropagated in LB broth containing the same concentration of antibioticsthen mixed with an equal volume of LB broth containing 30% (w/v)glycerol.

Media

The fermentation medium used for the production of recombinant proteinconsisted of 2×YT broth (Difco) containing 50 μg/ml Kn and 100 μg/ml Ap.Antifoam was added to medium for the fermentor at 0.25 ml/L (Antifoam204, Sigma). To induce expression of the BASB027 recombinant protein,IPTG (Isopropyl β-D-Thiogalactopyranoside) was added to the fermentor (1mM, final).

Fermentation

A 500-ml erlenmeyer seed flask, containing 50 ml working volume, wasinoculated with 0.3 ml of rapidly thawed frozen culture, or severalcolonies from a selective agar plate culture, and incubated forapproximately 12 hours at 37±1° C. on a shaking platform at 150 rpm(Innova 2100, New Brunswick Scientific). This seed culture was then usedto inoculate a 5-L working volume fermentor containing 2×YT broth andboth Kn and Ap antibiotics. The fermentor (Bioflo 3000, New BrunswickScientific) was operated at 37±1° C., 0.2-0.4 VVM air sparge, 250 rpm inRushton impellers. The pH was not controlled in either the flask seedculture or the fermentor. During fermentation, the pH ranged 6.5 to 7.3in the fermentor. IPTG (1.0 M stock, prepared in sterile water) wasadded to the fermentor when the culture reached mid-log of growth (˜0.7O.D.600 units). Cells were induced for 2-4 hours then harvested bycentrifugation using either a 28RS Heraeus (Sepatech) or RC5C superspeedcentrifuge (Sorvall Instruments). Cell paste was stored at −20° C. untilprocessed.

Purification Chemicals and Materials

Imidazole, guanidine hydrochloride, Tris (hydroxymethyl), and EDTA(ethylene-diamine tetraacetic acid) biotechnology grade or better wereall obtained from Ameresco Chemical, Solon, Ohio. Triton X-100(t-Octylphenoxypolyethoxy-ethanol), sodium phosphate, monobasic, andUrea were reagent grade or better and obtained from Sigma ChemicalCompany, St. Louis, Mo. Glacial acetic acid and hydrochloric acid wereobtained from Mallincrodt Baker Inc., Phillipsburg, N.J. Methanol wasobtained from Fisher Scientific, Fairlawn, N.J. Pefabloc®SC(4-(2-Aminoethyl)-benzenesulfonylfuoride), Complete protease inhibitorcocktail tablets, and PMSF (phenylmethyl-sulfonylfluoride) were obtainedfrom Roche Diagnostics Corporation, Indianapolis, Ind. Bestatin,Pepstatin A, and E-64 protease inhibitor were obtained from Calbiochem,LaJolla, Calif. Dulbecco's Phosphate Buffered Saline (1×PBS) wasobtained from Quality Biological, Inc., Gaithersburg, Md. Dulbecco'sPhosphate Buffered Saline (10×PBS) was obtained from BioWhittaker,Walkersville, Md. Penta-His Antibody, BSA free was obtained from QIAGEN,Valencia, Calif. Peroxidase-conjugated AffiniPure Goat Anti-mouse IgGwas obtained from Jackson Immuno Research, West Grove, Pa. AEC singlesolution was obtained from Zymed, South San Francisco, Calif. All otherchemicals were reagent grade or better.

Ni-NTA Superflow resin was obtained from QIAGEN Inc., Valencia, Calif.Precast Tris-Glycine 4-20% and 10-20% polyacrylamide gels, all runningbuffers and solutions, See Blue Pre-Stained Standards, MultiMarkMulti-Colored Standards and PVDF transfer membranes were obtained fromNovex, San Diego, Calif. SDS-PAGE Silver Stain kits were obtained fromDaiichi Pure Chemicals Company Limited, Tokyo, Japan. Coomassie StainSolution was obtained from Bio-Rad Laboratories, Hercules, Calif.Acrodisc® PF 0.2 m syringe filters were obtained from Pall GelmanSciences, Ann Arbor, Mich. GD/X 25 mm disposable syringe filters wereobtained from Whatman Inc., Clifton, N.J. Dialysis tubing 8,000 MWCO wasobtained from BioDesign Inc. Od New York, Carmal N.Y. BCA Protein AssayReagents and Snake Skin dialysis tubing 3,500 MWCO were obtained fromPierce Chemical Co., Rockford, Ill.

Extraction Protocol

Cell paste was thawed at room temperature for 30 to 60 minutes. Five tosix grams of material was weighed out into a 50 ml disposable centrifugetube. To this five mls/gram of Guanidine hydrochloride (Gu-HCl) bufferwas added (6 M Guanidine hydrochloride, 100 mM Sodium phosphate,monobasic, 10 mM Tris and 0.05% Triton X-100, pH 8.0). Cell paste wasresuspended using a PRO300D proscientific homogenizer, at ¾ power forone minute. The extraction mixture was then placed at room temperaturewith gentle agitation for 60 to 90 minutes. After 60 to 90 minutes theextraction mixture was centrifuged at 15,800×g for 15 minutes (SorvallRC5C centrifuge, 11,500 rpm). The supernatant (S1) was decanted andsaved for additional purification. The pellet (P1) was saved foranalysis.

Binding of BASB027 to Nickel-NTA Resin

To the S1 three to four mls of Ni-NTA resin is added. This is thenplaced at room temperature with gentle agitation for one hour. After onehour the S1/Ni-NTA is packed into an XK16 Pharmacia column. The columnis then washed with 1 M Gu-HCl buffer (1 M Guanidine hydrochloride, 100mM Sodium phosphate, monobasic, 10 mM Tris and 0.05% Triton X-100, pH8.0). This is then followed by a wash with phosphate buffer (100 mMSodium phosphate, monobasic, 10 mM Tris and 0.05% Triton X-100, pH 6.3).The protein is then eluted from the column with a 250 mM imidazolebuffer (250 mM imidazole, 100 mM sodium phosphate, monobasic, 10 mM Trisand 0.05% Triton X-100, pH 5.9).

Final Formulation

BASB027 was formulated by dialysis overnight against, three changes of0.1% Triton X-100 and 1×PBS, pH 7.4, to remove residual Gu-HCl andimidazole. The purified protein was characterized and used to produceantibodies as described below.

Biochemical Characterizations SDS-PAGE and Western Blot Analysis

The recombinant purified protein was resolved on 4-20% polyacrylamidegels and electrophoretically transferred to PVDF membranes at 100 V for1 hour as previously described (Thebaine et al. 1979, Proc. Natl. Acad.Sci. USA 76:4350-4354). The PVDF membranes were then pretreated with 25ml of Dulbecco's phosphate buffered saline containing 5% non-fat drymilk. All subsequent incubations were carried out using thispretreatment buffer.

PVDF membranes were incubated with 25 ml of a 1:500 dilution ofpreimmune serum or rabbit anti-His immune serum for 1 hour at roomtemperature. PVDF membranes were then washed twice with wash buffer (20mM Tris buffer, pH 7.5, containing 150 mM sodium chloride and 0.05%Tween-20). PVDF membranes were incubated with 25 ml of a 1:5000 dilutionof peroxidase-labeled goat anti-rabbit IgG (Jackson ImmunoResearchLaboratories, West Grove, Pa.) for 30 minutes at room temperature. PVDFmembranes were then washed 4 times with wash buffer, and were developedwith 3-amino-9-ethylcarbazole and urea peroxide as supplied by Zymed(San Francisco, Calif.) for 10 minutes each.

The results of an SDS-PAGE (FIG. 4) show a protein about 95 kDa that isreactive to an anti-RGS(His) antibody by western blots (FIG. 5) of theSDS-PAGE.

Protein Sequencing

Amino terminal amino acid sequencing of the purified protein wasperformed to confirm the production of the correct recombinant proteinusing well defined chemical protocols on Hewlett-Packard model G1000Asequencer with a model 1090 LC and a Hewlett-Packard model 241 sequencerwith a model 1100 LC.

Example 5 Production of Antisera to Recombinant BASB027

Polyvalent antisera directed against the BASB027 protein were generatedby vaccinating two rabbits with the purified recombinant BASB027protein. Each animal is given a total of three immunizationsintramuscullarly (i.m.) of about 20 μg BASB027 protein per injection(beginning with complete Freund's adjuvant and followed with incompleteFreund's adjuvant) at approximately 21 day intervals. Animals were bledprior to the first immunization (“pre-bleed”) and on days 35 and 57.

Anti-BASB027 protein titres were measured by an ELISA using purifiedrecombinant BASB027 protein (0.5 μg/well). The titre is defined as thehighest dilution equal to or greater than 0.1 as calculated with thefollowing equation: average OD of two test samples of antisera—theaverage OD of two test samples of buffer.

The antisera were used as the first antibody to identify the protein ina western blot as described in example 4 above. The western-blot showsthe presence of anti-BASB027 antibody in the sera of immunized animals(FIG. 6).

Example 6 Immunological Characterisation Western Blot Analysis

Several strains of M. catarrhalis were grown on chocolate agar platesfor 48 hours at 35° C. in 5% CO2. Several colonies were used toinoculate 25 ml of Muller Hinton broth in a 250 ml flask. Cultures weregrown overnight and collected by centrifugation. Cells were thensolubilized by suspending 30 μg of cells in 150 μl of PAGE sample buffer(360 mM Tris buffer, pH 8.8, containing 4% sodium dodecylsulfate and 20%glycerol), and incubating the suspension at 100° C. for 5 minutes. Thesolubilized cells were resolved on 4-20% polyacrylamide gels and theseparated proteins were electrophoretically transferred to PVDFmembranes at 100V for 1 hour as previously described (Thebaine et al.1979, Proc. Natl. Acad. Sci. USA 76:4350-4354). The PVDF membranes werethen pretreated with 25 ml of Dulbecco's phosphate buffered salinecontaining 5% non-fat dry milk. All subsequent incubations were carriedout using this pretreatment buffer.

PVDF membranes were incubated with 25 ml of a 1:500 dilution ofpreimmune serum or rabbit immune serum for 1 hour at room temperature.PVDF membranes were then washed twice with wash buffer (20 mM Trisbuffer, pH 7.5, containing 150 mM sodium chloride and 0.05% Tween-20).PVDF membranes were incubated with 25 ml of a 1:5000 dilution ofperoxidase-labeled goat anti-rabbit IgG (Jackson ImmunoResearchLaboratories, West Grove, Pa.) for 30 minutes at room temperature. PVDFmembranes were then washed 4 times with wash buffer, and were developedwith 3-amino-9-ethylcarbazole and urea peroxide as supplied by Zymed(San Francisco, Calif.) for 10 minutes each.

A protein of about 95 kDa (corresponding to BASB027 expected molecularweight) that is reactive with the antisera is detected in all Moraxellastrains (FIG. 7).

Bactericidal Activity

Complement-mediated cytotoxic activity of anti-BASB027 antibodies wasexamined to determine the vaccine potential of BASB027 polypeptide.Antiserum was prepared as described above. The activities of thepre-immune serum and the anti-BASB027 antiserum in mediating complementkilling of M. catarrhalis were examined using the “Serum BactericidalTest” described by Zollinger et al. (Immune Responses to Neisseriameningitis, in Manual of Clinical Laboratory Immunology, 3rd ed., pg347-349), except that cells of M. catarrhalis strains or cultivars wereused instead of Neisseria meningitis cells.

The bactericidal titer of rabbit antiserum (50% killing of homologousstrain) was <1:8 (pre-immune) and >1:128 (immune).

Example 7 Presence of Antibody to BASB027 in Human Convalescent Sera

Western blot analysis of purified recombinant BASB027 were performed asdescribed in Example 4 and 6 above, except that a pool of human serafrom children infected by M. catarrhalis was used as the first antibodypreparation. Results show that antisera from naturally infectedindividuals react to the purified recombinant.

Example 8 Production of BASB027 Peptides, Antisera and ReactivityThereof

Two short amino acid BASB027 specific peptides, having the sequences ofCYAKPLNKKQNDQTDT (SEQ ID NO:9) and YLTARRGQQTTLGEVVC (SEQ ID NO:10) wereproduced in the laboratory using generally well known methods. Thesepeptides coupled to KLH were used to produce antibodies in 12 weeks oldSpecific Pathogen Free New-Zealand female rabbits. Rabbits received 4injections at approximately 3 weeks intervals of 200 μg of peptide-KLHin complete (1^(st) injection) or incomplete (2^(nd), 3^(rd) and 4^(th)injections) Freund's adjuvant. Animals were bled prior to the firstimmunization and one month after the 4^(th) injection.

Anti-peptide mid-point titres were measured by an ELISA using freepeptides. Anti-peptide Mid-point titres one month after the 4^(th)immunization were superior to 15000.

Western blots of purified recombinant BASB027, using anti-peptideantibodies as the first antibody, were prepared as described in Example4 and 6. The results are presented in FIG. 8.

Deposited Materials

A deposit containing a Moraxella catarrhalis Catlin strain has beendeposited with the American Type Culture Collection (herein “ATCC”) onJun. 21, 1997 and assigned deposit number 43617. The deposit wasdescribed as Branhamella catarrhalis (Frosch and Kolle) and is afreeze-dried, 1.5-2.9 kb insert library constructed from M. catarrhalisisolate obtained from a transtracheal aspirate of a coal miner withchronic bronchitits. The deposit is described in Antimicrob. AgentsChemother. 21: 506-508 (1982).

The Moraxella catarrhalis strain deposit is referred to herein as “thedeposited strain” or as “the DNA of the deposited strain.”

The deposited strain contains a full length BASB027 gene.

A deposit of the vector pMC-D15 consisting of Moraxella catarrhalis DNAinserted in pQE30 has been deposited with the American Type CultureCollection (ATCC) on Feb. 12, 1999 and assigned deposit number 207105.

The sequence of the polynucleotides contained in the depositedstrain/clone, as well as the amino acid sequence of any polypeptideencoded thereby, are controlling in the event of any conflict with anydescription of sequences herein.

The deposit of the deposited strains have been made under the terms ofthe Budapest Treaty on the International Recognition of the Deposit ofMicro-organisms for Purposes of Patent Procedure. The deposited strainswill be irrevocably and without restriction or condition released to thepublic upon the issuance of a patent. The deposited strains are providedmerely as convenience to those of skill in the art and are not anadmission that a deposit is required for enablement, such as thatrequired under 35 U.S.C.§112.

1.-13. (canceled)
 14. An isolated polynucleotide encoding a polypeptideor the full complement to the isolated polynucleotide, wherein thepolypeptide is selected from (a) a polypeptide comprising an amino acidsequence at least 90% identical to the amino acid sequence set forth inSEQ ID NO:2 or SEQ ID NO:4; (b) a polypeptide comprising an amino acidsequence at least 95% identical to the amino acid sequence set forth inSEQ ID NO:2 or SEQ ID NO:4; or (c) a polypeptide comprising animmunogenic fragment that is at least 15 contiguous amino acids of theamino acid sequence set forth in SEQ ID NO:2 or SEQ ID NO:4.
 15. Theisolated polynucleotide of claim 14, wherein the isolated polynucleotideencodes a polypeptide comprising the amino acid sequence set forth inSEQ ID NO:2 or SEQ ID NO:4.
 16. The isolated polynucleotide of claim 14comprising the nucleotide sequence set forth in SEQ ID NO:1 or SEQ IDNO:3.
 17. An isolated polynucleotide segment comprising a polynucleotidesequence or the full complement of the entire length of thepolynucleotide sequence, wherein the polynucleotide sequence hybridizesto the full complement of SEQ ID NO:1 or SEQ ID NO:3 minus thecomplement of any stop codon, wherein the hybridization conditionsinclude incubation at 42° C. in a solution comprising 50% formamide,5×SSC (150 mM NaCl, 15 mM trisodium citrate), 50 mM sodium phosphate(pH7.6), 5×Denhardt's solution, 10% dextran sulfate, and 20micrograms/ml denatured, sheared salmon sperm DNA, followed by washingin 0.1×SSC at 65° C.; and, wherein the polynucleotide sequence isidentical to SEQ ID NO:1 or SEQ ID NO:3 minus any terminal stop codon,except that, over the entire length corresponding to SEQ ID NOs:1 or 3minus any terminal stop codon, n_(n) nucleotides are substituted,inserted or deleted, wherein n_(n) satisfies the following expressionn _(n) ≦x _(n)−(x _(n) •y), wherein x_(n) is the total number ofnucleotides in SEQ ID NO:1 or SEQ ID NO:3 minus any terminal stop codon,y is at least 0.95, and wherein any non-integer product of x_(n) and yis rounded down to the nearest integer before subtracting the productfrom x_(n); and wherein the polynucleotide sequence detects Moraxellacatarrhalis.
 18. An expression vector comprising the isolatedpolynucleotide of claim
 14. 19. A host cell transformed with theexpression vector of claim
 18. 20. A process of producing an isolatedpolypeptide comprising (a) culturing the host cell of claim 19 underconditions sufficient for the production of the encoded polypeptide and(b) recovering the polypeptide.
 21. A nucleic acid vaccine comprisingthe isolated polynucleotide of claim 14 and a pharmaceuticallyacceptable carrier.
 22. An isolated polynucleotide segment comprising apolynucleotide sequence or the full complement of the entire length ofthe polynucleotide sequence, wherein the polynucleotide sequence isidentical to SEQ ID NO:1 or SEQ ID NO:3 minus any terminal stop codon,except that, over the entire length corresponding to SEQ ID NO:1 or SEQID NO:3 minus any terminal stop codon n_(n) nucleotides are substituted,inserted or deleted, wherein n_(n) satisfies the following expressionn _(n) ≦x _(n)−(x _(n) •y), wherein x_(n) is the total number ofnucleotides in SEQ ID NO:1 or SEQ ID NO:3 minus any terminal stop codony is at least 0.90, and wherein any non-integer product of x_(n) and yis rounded down to the nearest integer before subtracting the productfrom x_(n); and wherein the polynucleotide sequence detects Moraxellacatarrhalis.
 23. The isolated polynucleotide of claim 22 wherein y is atleast 0.95.
 24. An expression vector comprising the isolatedpolynucleotide of claim 22 which codes for a polypeptide that, whenadministered to a mammal induces an immune response that recognizes apolypeptide consisting of the amino acid sequence of SEQ ID NO:2 or SEQID NO:4.
 25. A host cell transformed with (a) the isolatedpolynucleotide of claim 22 or (b) an expression vector comprising theisolated polynucleotide of claim
 22. 26. A process of producing anisolated polypeptide comprising (a) culturing the host cell of claim 25under conditions sufficient for the production of the encodedpolypeptide and (b) recovering the polypeptide. 27.-33. (canceled)
 34. Aprocess for expressing the isolated polynucleotide of claim 14comprising transforming a host cell with an expression vector comprisingthe polynucleotide and culturing the host cell under conditionssufficient for expression of the polynucleotide.